<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
					<div>
			<div></div>
		</div>
				</div>
				</div>
				<div>
				<div>
			
				</div>
				<div>
				<div>
					<div><p>The Emergency Care Worker Diploma is a comprehensive course that will prepare you for a career in emergency care. You'll learn about the different types of emergencies, how to assess and treat patients, and how to provide life support. You'll also learn about the latest medical equipment and procedures, and how to work as part of a team to deliver the best possible care.</p><p>Your journey begins with an Introduction to Emergency Care Worker, where you'll be captivated by the importance of your role in saving lives. As you progress, you'll step into Section 02, where you'll learn the art of Emergency Care Assistant Driving and Assisting the Clinician, a skill that can make all the difference in life-or-death situations. The adrenaline will surge as you dive into topics like Catastrophic Bleeding, Airway Management, Primary Survey, Secondary Survey, Medical Gases, and Basic First-Aid Techniques. These sections will provide you essential and exhilarating knowledge.</p><p>As the course unfolds, you'll find yourself immersed in the art of handling Minor Injuries at the Workplace, mastering Secondary Illness Loss of Responsiveness and CPR, and confidently addressing Secondary Illness Breathing Problems. You'll become the linchpin in Trauma Emergencies and acquire the expertise to manage Fractures and Dislocations. Moreover, you'll understand Reporting Requirements and Identification, crucial for accurate record-keeping in emergency situations. Additionally, you'll gain insights into European Regulations on Medical Devices and the Quality System in Medical Device Regulation, ensuring that you're well-versed in the regulatory landscape.</p><p>By the time you complete this diploma, you will be armed with theoretical knowledge and the confidence to act swiftly and decisively in high-pressure scenarios. Join us in this transformative journey, and let's make you the hero communities rely on in times of need. Your future as a skilled and compassionate Emergency Care Worker awaits.</p></div>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</div></section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2><b> Learning outcome</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Assess patients in an emergency situation</span>
									</li>
								<li>
											<span>
													</span>
										<span>Provide basic life support</span>
									</li>
								<li>
											<span>
													</span>
										<span>Manage common medical and surgical emergencies</span>
									</li>
								<li>
											<span>
													</span>
										<span>Drive an emergency vehicle</span>
									</li>
								<li>
											<span>
													</span>
										<span>Assist a clinician in an emergency situation</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
					</div>
				</div>
				<div>
				<div>
					<div>
							
					
									
							
					
									
							
					
									
							
					
									
					</div>
			</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Why should I take this course?</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Gain life-saving skills and make a difference in emergencies.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Enhance your career prospects in the healthcare sector.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Become a valued asset in various medical settings.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Acquire knowledge compliant with European medical device regulations.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Boost your confidence in handling critical situations.</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Career Path</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Emergency Medical Technician</span>
									</li>
								<li>
											<span>
													</span>
										<span>Paramedic</span>
									</li>
								<li>
											<span>
													</span>
										<span>Ambulance Care Assistant</span>
									</li>
								<li>
											<span>
													</span>
										<span>First Aid Trainer</span>
									</li>
								<li>
											<span>
													</span>
										<span>Healthcare Assistant</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Requirements</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>High school diploma or equivalent.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Basic knowledge of human anatomy and physiology.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Access to a computer with internet connectivity.</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section><div>
                            <div>
                                <h2>Course Curriculum</h2>
                            </div>
                            			<div>
				

<div>
<table width="100%">				<tbody><tr>
					<td colspan="4"><strong>Section 01: Introduction to Emergency Care Worker</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Introduction to Emergency Care Worker</td><td><span>🕐 00:11:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 02: Emergency Care Assistant Driving and Assisting the Clinician</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Emergency Care Assistant Driving and Assisting the Clinician</td><td><span>🕐 00:11:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 03: Catastrophic Bleeding</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Catastrophic Bleeding</td><td><span>🕐 00:15:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 04: Airway Management</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Airway Management</td><td><span>🕐 00:20:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 05: Primary Survey</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Primary Survey</td><td><span>🕐 00:11:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 06: Secondary Survey</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Secondary Survey</td><td><span>🕐 00:14:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 07: Medical Gases</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Medical Gases</td><td><span>🕐 00:15:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 08: Basic First-Aid Techniques</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Basic First-Aid Techniques</td><td><span>🕐 00:27:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 09: Dealing with Minor Injuries at the Workplace</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Dealing with Minor Injuries at the Workplace</td><td><span>🕐 00:40:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 10: Secondary Illness Loss of Responsiveness and CPR</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Secondary Illness Loss of Responsiveness and CPR</td><td><span>🕐 00:12:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 11: Secondary Illness Breathing Problems</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Secondary Illness Breathing Problems</td><td><span>🕐 00:10:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 12: Secondary Illnesses and Injuries</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Secondary Illnesses and Injuries</td><td><span>🕐 00:20:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 13: Dealing With Fractures and Dislocations</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Dealing With Fractures and Dislocations</td><td><span>🕐 00:10:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 14: Trauma Emergencies</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Trauma Emergencies</td><td><span>🕐 00:20:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 15: Reporting Requirements and Identification</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Reporting Requirements and Identification</td><td><span>🕐 00:16:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 16: Overview to European Regulations on Medical Devices</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Overview to European Regulations on Medical Devices</td><td><span>🕐 00:33:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 17: Quality System in Medical Device Regulation</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Quality System in Medical Device Regulation</td><td><span>🕐 00:25:00</span></td>
				</tr>
				</tbody></table></div>

			</div>
		                        </div>

Skill Up

Certificate in Emergency Response Ambulance Driving (CERAD)

Emergency Care Assistant

Paramedic Training

Apprentice Emergency Medical Technician (AEMT)

Ambulance First Aid

Emergency First Aid

Learn the skills to provide essential care in emergency situations. This diploma will prepare you for a rewarding career in emergency care, helping people in need when they need it most.

Emergency Care Worker Diploma

General Admission

<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
					<div>
			<div></div>
		</div>
				</div>
				</div>
				<div>
				<div>
			
				</div>
				<div>
				<div>
					<div><p>Gain the skills and credentials to kickstart a successful career and learn from the experts with this step-by-step training course. This European Medical Device Regulations  has been specially designed to help learners gain a good command of European Medical Device Regulations , providing them with a solid foundation of knowledge to become a qualified professional.</p><p>Through this European Medical Device Regulations , you will gain both practical and theoretical understanding of European Medical Device Regulations  that will increase your employability in this field, help you stand out from the competition and boost your earning potential in no time.</p><p>Not only that, but this training includes up-to-date knowledge and techniques that will ensure you have the most in-demand skills to rise to the top of the industry. This qualification is fully accredited, broken down into several manageable modules, ideal for aspiring professionals.</p></div>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</div></section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2><b> Learning outcome</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Familiar yourself with the recent development and updates of the relevant industry</span>
									</li>
								<li>
											<span>
													</span>
										<span>Know how to use your theoretical knowledge to adapt in any working environment</span>
									</li>
								<li>
											<span>
													</span>
										<span>Get help from our expert tutors anytime you need</span>
									</li>
								<li>
											<span>
													</span>
										<span>Access to course contents that are designed and prepared by industry professionals</span>
									</li>
								<li>
											<span>
													</span>
										<span>Study at your convenient time and from wherever you want</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
					</div>
				</div>
				<div>
				<div>
					
			</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Why should I take this course?</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Affordable premium-quality E-learning content, you can learn at your own pace.</span>
									</li>
								<li>
											<span>
													</span>
										<span>You will receive a completion certificate upon completing the course.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Internationally recognized Accredited Qualification will boost up your resume.</span>
									</li>
								<li>
											<span>
													</span>
										<span>You will learn the researched and proven approach adopted by successful people to transform their careers.</span>
									</li>
								<li>
											<span>
													</span>
										<span>You will be able to incorporate various techniques successfully and understand your customers better.</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Requirements</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>No formal qualifications required, anyone from any academic background can take this course.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Access to a computer or digital device with internet connectivity.</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section><div>
                            <div>
                                <h2>Course Curriculum</h2>
                            </div>
                            			<div>
				

<div>
<table width="100%">				<tbody><tr>
					<td colspan="4"><strong>Module 1: Overview to European Regulations on Medical Devices</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Overview to European Regulations on Medical Devices</td><td><span>🕐 00:45:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Module 2: Essential Components of EU MDR</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Essential Components of EU MDR</td><td><span>🕐 00:42:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Module 3: Reporting Requirements and Identification</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Reporting Requirements and Identification</td><td><span>🕐 00:29:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Module 4: Quality System in Medical Device Regulation</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Quality System in Medical Device Regulation</td><td><span>🕐 00:38:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Mock Exam</strong></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Mock Exam - European Medical Device Regulations</td><td><span>🕐 00:20:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Final Exam</strong></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Final Exam - European Medical Device Regulations</td><td><span>🕐 00:20:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Order Your Certificate</strong></td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Order Your Certificate</td><td><span>🕐 00:00:00</span></td>
				</tr>
				</tbody></table></div>

			</div>
		                        </div>

Certificate in Further Education & Training (Cert Ed)

Medical Training

Certificate in Education & Training (CET)

European Computer Driving Licence (ECDL)

Trainers Course

Medical Education

Gain the skills and credentials to kickstart a successful career and learn from the experts with this step-by-step

European Medical Device Regulations

<p>Unlock the secrets to navigating the intricate landscape of European medical device regulations with our comprehensive course. Designed for those who seek mastery in understanding and applying the latest EU standards, this course is your gateway to compliance excellence. Dive deep into the regulatory environment, where you'll explore the essential components that govern the medical device industry in Europe. Learn how to seamlessly integrate these regulations into your practice, ensuring your products meet the highest standards of safety and efficacy.</p><p><strong>Key Features:</strong></p><ul><li>CPD Certified </li><li>Free Certificate from Reed</li><li>CIQ Approved</li><li>Developed by Specialist</li><li>Lifetime Access </li></ul><p>Discover the nuances of reporting requirements and identification processes, critical for maintaining transparency and accountability. Our expertly curated content guides you through establishing a robust quality system, pivotal for regulatory success. Equip yourself with the knowledge to confidently manage regulatory submissions and navigate quality audits with ease. Join a community of like-minded professionals and elevate your regulatory expertise, ensuring your organisation stays ahead in the competitive medical device market. Enrol now to transform your approach to European medical device regulations and lead with confidence in a compliant and efficient manner.</p><p><strong>Course Curriculum</strong></p><ul><li>Module 01: Overview to European Regulations on Medical Devices</li><li>Module 02: Essential Components of EU MDR</li><li>Module 03: Reporting Requirements and Identification</li><li>Module 04: Quality System in Medical Device Regulation</li></ul><p><strong>Learning Outcomes:</strong></p><ul><li>Understand the core elements of European medical device regulations.</li><li>Identify key components of EU Medical Device Regulation (MDR).</li><li>Master reporting requirements and device identification processes.</li><li>Implement quality systems in medical device regulation.</li><li>Analyse essential EU MDR regulatory requirements.</li><li>Navigate the complexities of EU medical device compliance.</li></ul><h2>
        
        <div>CPD</div>
    </h2>

                        <div id="cpd">
                            <div>
                                <div>
                                    <div>
                                        10 CPD hours / points
                                    </div>
                                        <div>
                                            Accredited by CPD Quality Standards
                                        </div>
                                </div>
                            </div>
                        </div><li>
                                        <h3>
                                            
                                                Essential Components of European Medical Device Regulations <span>1:45:07</span>
                                                <span></span>
                                            
                                        </h3>
                                        <ul id="section1">
                                                <li>
                                                    <span>1: Module 01: Overview to European Regulations on Medical Devices		</span>

                                                    <span>33:17</span>

                                                        
                                                                                                                                                                                                            </li>
                                                <li>
                                                    <span>2: Module 02: Essential Components of EU MDR		</span>

                                                    <span>29:12</span>

                                                        
                                                                                                                                                                                                            </li>
                                                <li>
                                                    <span>3: Module 03: Reporting Requirements and Identification		</span>

                                                    <span>16:21</span>

                                                        
                                                                                                                                                                                                            </li>
                                                <li>
                                                    <span>4: Module 04: Quality System in Medical Device Regulation</span>

                                                    <span>25:17</span>

                                                        
                                                                                                                                                                                                            </li>
                                                <li>
                                                    <span>5: CPD Certificate - Free</span>

                                                    <span>01:00</span>

                                                                                                                                                                
                                                                                                    </li>
                                        </ul>
                                    </li><h2>
        
        <div>Who is this course for?</div>
    </h2>

                        <div id="who_is_this_course_for">
                            <ul><li>Regulatory affairs specialists in the medical device industry.</li><li>Quality assurance professionals in healthcare.</li><li>Compliance officers in medical device companies.</li><li>Medical device product managers.</li><li>Legal advisors in healthcare regulation.</li></ul>
                        </div><h2>
        
        <div>Career path</div>
    </h2>

                        <div id="career_path">
                            <ul><li>Regulatory Affairs Specialist</li><li>Quality Assurance Manager</li><li>Compliance Officer</li><li>Medical Device Consultant</li><li>Product Manager</li><li>Regulatory Affairs Associate</li></ul>
                        </div><h2>
        
        <div>Certificates</div>
    </h2>

                        <div id="optional_extras">
                                    <h4>Digital certificate</h4>
        <p>
            Digital certificate -
            Included
        </p>
        <h4>Reed Courses Certificate of Completion</h4>
        <p>
            Digital certificate -
            Included
        </p>
            <div><p>Will be downloadable when all lectures have been completed.</p></div>

                        </div>

Online Training Academy

Essential Components of European Medical Device Regulations

<h2>Description</h2><p><span><strong>Sterile Services Technician Diploma</strong></span></p><p><span>Sterile services technicians provide equipment and materials required by hospitals to carry out their various duties. These technicians collect reusable instruments from operating theatres, wards and clinics, disinfect them and make sure that they are clean and working properly. The sterilised instruments are then delivered to the hospital by trolley.</span></p><p><span>The work of sterile service technicians begins by assembling instruments and supplying items like dressings, syringes and needles and arranging them in trays or packs according to standard procedures. The packs or trays are sealed, labelled and sterilised in steam. Large items of medical equipment are disinfected with the help of specialised equipment.</span></p><p><span>Sterile services Technicians generally work as a team and are considered to be an integral part of the healthcare team. They report to the manager of the sterile services department (also referred to as decontamination service) and their services are available 37 hours a week. In larger departments, staff may provide their services 24/7, in which case staff may be employed in shifts.</span></p><p><span>Sterile services departments can be found within hospitals or separately, and they could be run by commercial providers or hospital management. A sterile services technician can, with experience, climb to the position of assistant manager and then on to service management.</span></p><p><span>Sterile services technicians can be found mostly at National Health Service (NHS) hospitals around the UK, but they are also found at private hospitals, health centres and dental practices. The sterile services sector presently employs around 20,000 people, and there are always vacancies in this field, which can be found in the local press or NHS website. Information regarding vacancies in this sector can also be found at Jobcentre Plus Offices.</span></p><p><span>The course in sterile services technician covers prevention and control of infections, transporting and containment of reusable medical devices, cleaning and disinfecting equipment, assembly and packaging, function testing, inspection, sterilisation and storage and distribution of equipment.</span></p><p><span><strong>What you will learn</strong></span></p><p><span><strong>1:</strong> Overview</span><br />
<span><strong>2:</strong> Cleaning and Packaging</span><br />
<span><strong>3:</strong> Sterilization</span><br />
<span><strong>4:</strong> Quality Management in Sterilizing Services</span><br />
<span><strong>5:</strong> Thermal and Chemical Disinfection</span></p><h4>Course Outcomes</h4><p>
After completing the course, you will receive a diploma certificate and an academic transcript from Elearn college.</p><h4>Assessment</h4><p>
Each unit concludes with a multiple-choice examination. This exercise will help you recall the major aspects covered in the unit and help you ensure that you have not missed anything important in the unit. The results are readily available, which will help you see your mistakes and look at the topic once again. If the result is satisfactory, it is a green light for you to proceed to the next chapter.</p><h4>Accreditation</h4><p>
Elearn College is a registered Ed-tech company under the UK Register of Learning( Ref No:10062668). After completing a course, you will be able to download the certificate and the transcript of the course from the website. For the learners who require a hard copy of the certificate and transcript, we will post it for them for an additional charge.</p>

Elearncollege

Sterile services Course

<p>A laboratory technician is a healthcare professional who performs laboratory tests and experiments to diagnose and treat various medical conditions. They work in a variety of settings, and their primary responsibility is to collect and analyse patient specimens. To become a laboratory technician, you will need a high school diploma or equivalent and complete a laboratory technician program.</p><p>The program typically lasts 1-2 years and includes both classroom and hands-on training. Laboratory technicians require strong analytical and critical thinking skills, attention to detail, and the ability to work in a team. The job outlook for laboratory technicians is positive, with an expected growth rate of 7% over the next 10 years.</p><p><strong>Highlights of The Certificate of Achievement Endorsed by the Quality Licence Scheme included with this Package:</strong></p><ul><li>The Quality Licence Scheme ensures that the course, you are enrolled in, is of the highest quality.</li><li>It helps you to easily get recognised by employers.</li><li>The endorsed certificate for this course will make you stand out from the crowd when applying for jobs during this pandemic.</li><li>The Certificate of Achievement Endorsed by the Quality Licence Scheme has already helped thousands of people to reach their professional goals and get better jobs.</li></ul><p><strong>Why People Enrol this course from One Education:</strong></p><ul><li>Receive a Quality Licence Scheme-endorsed certificate upon successful completion of the course</li><li>Learning materials for our course contain engaging voice-over and visual elements for your comfort</li><li>Get 24/7 access to all content for a full year</li><li>Complete the course at your own pace</li><li>Each of our students gets full tutor support on weekdays (Monday to Friday)</li><li>Efficient assessments and instant results upon completion</li></ul><p>This masterclass Laboratory Technician Diploma at QLS Level 3 online training course is designed by industry experts and will give you an in-depth understanding of this topic. The Course features easy-to-digest modules that break down each topic and ensure all our students receive an unrivalled and thorough learning experience.</p><p>If you want to work in this rapidly growing sector and stand out from the competition, then our course is the perfect place to kickstart your dream career.</p><p><strong>Course Curriculum:</strong></p><p>Here is a curriculum breakdown of the course:</p><p><strong>Module 01: Introduction to Laboratory Technician</strong></p><ul><li>Introduction to the Course</li><li>History of medical laboratory science</li><li>What is a Laboratory</li><li>Types of Laboratories</li><li>Classification of Laboratories</li><li>Classification of Medical Laboratories</li><li>Laboratory Organisation</li><li>Structure and Activities of Medical Laboratory Services</li></ul><p><strong>Module 02: Medical Laboratory Services</strong></p><ul><li>Role of Medical Laboratory Services</li><li>Major Roles of a Medical Laboratory Technologist</li><li>Rules &amp; Regulations of Medical Laboratory</li><li>Medical Laboratory Request Forms</li><li>Delivery of laboratory results</li><li>Professional code of conduct and ethics</li><li>Standard Laboratory Policies</li><li>Laboratory hour and emergency work</li><li>The range of tests to be performed and those to be referred to a higher level</li><li>Collection of laboratory specimen</li><li>Workload capacity of a laboratory</li></ul><p><strong>Module 03: Laboratory Equipments</strong></p><ul><li>Introduction</li><li>Autoclaves, Ovens, Incubators, and Water-Baths</li><li>Use of Autoclaves</li><li>Periodic inspection and cleaning</li><li>Hot-Air Ovens</li><li>Incubators</li><li>Water-Baths</li><li>Balances</li><li>Mechanical Balances</li><li>Electromagnetic Balances</li><li>Good Working Practices-All Balances</li><li>Unpacking, Siting, and Installation</li><li>Special Tools/Spares/Requirements</li><li>Batteries</li><li>Recharging Lead-Acid Batteries</li><li>Gas Cylinders and Gases</li><li>Pipettes, Autopipettes, and Dispensers</li><li>Refrigerators</li></ul><p><strong>Module 04: How to Work with Microscope</strong></p><ul><li>Introduction to Microscope</li><li>Purpose of the Equipment</li><li>Installation Requirements</li><li>Description of Potential Problems with Microscopes</li><li>Eyepieces</li><li>Binocular Head</li></ul><p><strong>Module 05: Solutions Used in Medical Laboratory</strong></p><ul><li>Solution, Solute and Solvent</li><li>Reagent Solutions</li><li>Staining solutions</li><li>Standard solutions</li><li>Buffer solutions</li></ul><p><strong>Module 06: Sterilisation, Disinfection and Decontamination</strong></p><ul><li>Definition</li><li>The process of sterilisation</li><li>Physical Methods of Sterilisation</li><li>Dry heat</li><li>Moist heat</li></ul><p><strong>Module 07: How to Decontaminate Reusable Medical Devices</strong></p><ul><li>The Decontamination Cycle</li><li>Acquisition</li><li>Cleaning</li><li>Automated Cleaning</li><li>Storage of Sterile Medical Devices</li></ul><p><strong>Module 08: Laboratory Accidents and Safety</strong></p><ul><li>Chemical hazards</li><li>Physical Hazards</li><li>Additional Laboratory Hazards</li><li>Infection.</li></ul><p><strong>Module 09: Quality Assurance</strong></p><ul><li>The importance of quality assurance</li><li>Types and causes of errors in medical laboratories</li><li>The steps of the quality assurance program</li></ul><p><strong>Module 10: Standard Operating Procedures</strong></p><ul><li>Standard Operating Procedures</li><li>Effective Standard Operating Procedures</li><li>Provision and Use of Personal Protective Equipment (PPE)</li><li>Gloves</li><li>Eye Protection</li></ul><p><strong>Module 11: Glossary</strong></p><ul><li>Different types of glossaries used in the medical laboratory</li></ul><p><strong>How is the course assessed?</strong></p><p>To simplify the procedure of evaluation and accreditation for learners, we provide an automated assessment system. Upon completion of an online module, you will immediately be given access to a specifically crafted MCQ test. The results will be evaluated instantly, and the score displayed for your perusal. For each test, the pass mark will be set to 60%.</p><p>When all tests have been successfully passed, you will be able to claim a certificate endorsed by the Quality Licence Scheme.</p><p><strong>Certificate of Achievement</strong></p><p><strong>Endorsed Certificate of Achievement from the Quality Licence Scheme</strong></p><p>After successfully completing the course, learners will get an endorsed certificate (included with the course) delivered right at their doorstep by post, without paying a single penny! Please note that learners residing outside the UK have to pay a £10 postage charge.</p><p><strong>CPD Accredited Certification from One Education</strong></p><p>After successfully completing the MCQ assessment of this course, you will also qualify for a CPD Accredited Certificate from One Education, as proof of your continued professional development. Certification is available in PDF format, at the cost of £9, or a hard copy can be sent to you via post, at the cost of £15.</p><h2>
        
        <div>CPD</div>
    </h2>

                        <div id="cpd">
                            <div>
                                <div>
                                    <div>
                                        120 CPD hours / points
                                    </div>
                                        <div>
                                            Accredited by CPD Quality Standards
                                        </div>
                                </div>
                            </div>
                        </div><h2>
        
        <div>Who is this course for?</div>
    </h2>

                        <div id="who_is_this_course_for">
                            <p>The Laboratory Technician Diploma at QLS Level 3 training is ideal for highly motivated individuals who want to enhance their professional skills and train for the job they want! This course also suits people aspiring for some in-depth knowledge on this topic and keeping up to date with the latest information.</p><p>Study the Laboratory Technician Diploma at QLS Level 3 today and increase your professional skillset from the comfort of your home!</p>
                        </div><h2>
        
        <div>Requirements</div>
    </h2>

                        <div id="requirements">
                            <p>There are no formal entry requirements for the Laboratory Technician Diploma at QLS Level 3, with enrollment open to anyone!<strong> Anyone and everyone</strong> with a knack for learning can enrol on this course without any hesitation.</p><p>Learn online from any internet device, including your computer, tablet or smartphone. Study when it suits you and complete the course at your own pace.</p><p>All students must have a passion for learning and literacy, as well as being over the age of 16.</p>
                        </div><h2>
        
        <div>Career path</div>
    </h2>

                        <div id="career_path">
                            <p>Learn the essential skills and knowledge you need to exceed in your professional life with the help &amp; guidance from our online course.</p><ul><li>Laboratory Technician</li><li>Medical Laboratory Technician</li><li>Research Laboratory Technician</li><li>Clinical Laboratory Technician</li><li>Pathology Laboratory Technician</li><li>Quality Control Laboratory Technician</li><li>Biomedical Laboratory Technician</li><li>Analytical Laboratory Technician</li></ul>
                        </div>

One Education

Laboratory Technician Diploma at QLS Level 3 Course

<strong>Linkerd is a service mesh for Kubernetes. It makes running services easier and safer by giving you runtime debugging, observability, reliability, and security-all without requiring any changes to your code.</strong>
        <p>Linkerd is a different kind of service mesh that is ultra-light, ultra-simple, ultra-powerful. Linkerd adds security, observability, and reliability to Kubernetes, without the complexity. It's CNCF-hosted and 100% open source.

Linkerd works by installing a set of ultralights, transparent proxies next to each service instance. These proxies automatically handle all traffic to and from the service. Because they're transparent, these proxies act as highly instrumented out-of-process network stacks, sending telemetry to, and receiving control signals from, the control plane. This design allows Linkerd to measure and manipulate traffic to and from your service without introducing excessive latency.

In order to be as small, lightweight, and safe as possible, Linkerd's proxies are written in Rust and specialized for Linkerd. You can learn more about the proxies in the Linkerd proxy repo. It is a must tool for everyone who is working with microservices especially when working with Kubernetes.

By the end of the course, you will be able to understand how Linkerd works and learn to install CLI manually.</p>
        <h2>What You Will Learn</h2><p>Understand how to configure Linkerd<br>Learn how to inject Linkerd into your custom applications<br>Introduction to service mesh<br>Learn how to install CLI manually and deploy an application<br>Learn how to install flagger for canary release<br>Deploy Nextcloud application and inject Linkerd manually to collect metrics</p>
        <h2>Audience</h2><p>This course is for anyone who wants to become a DevOps engineer. It is designed for absolute beginners. No programming experience is needed.</p>
        <h2>Approach</h2><p>The course follows a learn by doing approach with live implementations.</p>
        <h2>Key Features</h2><p>Learn how to deploy a custom application and inject Linkerd manually * Explore progressive delivery operator for Kubernetes * Easy-to-watch video tutorials on how to install the Linkerd CLI manually</p>
        
        <h2>About the Author</h2><h3>Himanshu Sharma</h3><p>Himanshu Sharma is an expert in Kubernetes, containers, and cloud-native infrastructure. He has more than 12 years of IT experience in a variety of industries, including medical devices, entertainment, enterprise software, and cloud computing. He is passionate about learning new technologies and believes the best way to learn is by doing it practically.</p>
        <h2>Course Outline</h2><h4>1. Introduction</h4><p></p><br><h4>2. Getting Started - Install the linkerd CLI</h4><p></p><br><h4>3. Deploy custom application and inject Linkerd manually</h4><p></p><br><h4>4. Flagger ( Progressive Delivery Operator for Kubernetes )</h4><p></p><br><h4>5. Inject Proxy (DataPlane) both ways</h4><p></p><br><h4>6. Thank You</h4><p></p>

Packt

Kubernetes

Programming

Linkerd is a service mesh for Kubernetes. It makes running services easier and safer by giving you runtime debugging, observability, reliability, and security-all without requiring any changes to your code.

Linkerd - Service Mesh for Kubernetes

<div>
						<div>
				<div>
									<section>
						<div>
							<div>
					<div>
			<div>
							<div>
						<div>
				<div>
								<div>
				<p><span>Register on the Essentials of European Medical Device Regulations today and build the experience, skills and knowledge you need to enhance your professional development and work towards your dream job. Study this course through online learning and take the first steps towards a long-term career.</span></p><p><span>The course consists of a number of easy to digest, in-depth modules, designed to provide you with a detailed, expert level of knowledge. Learn through a mixture of instructional video lessons and online study materials.</span></p><p><span>Receive online tutor support as you study the course, to ensure you are supported every step of the way. Get an e-certificate as proof of your course completion.</span></p><p><span>The Essentials of European Medical Device Regulations is incredibly great value and allows you to study at your own pace. Access the course modules from any internet-enabled device, including computers, tablet, and smartphones.</span></p><p><span>The course is designed to increase your employability and equip you with everything you need to be a success. Enrol on the now and start learning instantly!</span></p><h5><b>What You Get With The Essentials of European Medical Device Regulations </b></h5><ul><li><span>Receive a e-certificate upon successful completion of the course</span></li><li><span>Get taught by experienced, professional instructors</span></li><li><span>Study at a time and pace that suits your learning style</span></li><li><span>Get instant feedback on assessments </span></li><li><span>24/7 help and advice via email or live chat</span></li><li><span>Get full tutor support on weekdays (Monday to Friday)</span></li></ul>					</div>
						</div>
				</div>
						</div>
					</div>
		</div>
								</div>
					</div>
		</section>
				<section>
						<div>
							<div>
					<div>
			<div>
							<div>
						<div>
				<div>
					<div>
							
					<div></div>
											<div></div>
														
							
					<div></div>
											<div></div>
														
							
					<div></div>
											<div></div>
														
							
					<div></div>
											<div></div>
														
					</div>
			</div>
				</div>
						</div>
					</div>
		</div>
								</div>
					</div>
		</section>
				<section>
						<div>
							<div>
					<div>
			<div>
							<div>
						<div>
				<div>
			<h2>Course Design</h2>		</div>
				</div>
				<div>
				<div>
								<div>
				<div id="course-home"><div><p><span>The course is delivered through our online learning platform, accessible through any internet-connected device. There are no formal deadlines or teaching schedules, meaning you are free to study the course at your own pace.</span></p><p><span>You are taught through a combination of</span></p><ul><li><span>Video lessons</span></li><li><span>Online study materials</span></li></ul></div></div>					</div>
						</div>
				</div>
						</div>
					</div>
		</div>
								</div>
					</div>
		</section>
				<section>
						<div>
							<div>
					<div>
			<div>
							<div>
						<div>
				<div>
			<h2>Certification</h2>		</div>
				</div>
				<div>
				<div>
								<div>
				<p><span>Upon successful completion of the course, you will be able to obtain your course completion e-certificate free of cost. Print copy by post is also available at an additional cost of £9.99 and PDF Certificate at £4.99.</span></p>					</div>
						</div>
				</div>
				<div>
				<div>
			<h2>Who Is This Course For:</h2>		</div>
				</div>
				<div>
				<div>
								<div>
				<p><span>The course is ideal for those who already work in this sector or are an aspiring professional. This course is designed to enhance your expertise and boost your CV. Learn key skills and gain a professional qualification to prove your newly-acquired knowledge.</span></p>					</div>
						</div>
				</div>
						</div>
					</div>
		</div>
								</div>
					</div>
		</section>
				<section>
						<div>
							<div>
					<div>
			<div>
							<div>
						<div>
				<div>
			<h2>Requirements:</h2>		</div>
				</div>
				<div>
				<div>
								<div>
				<p><span>The online training is open to all students and has no formal entry requirements. To study the Essentials of European Medical Device Regulations, all your need is a passion for learning, a good understanding of English, numeracy, and IT skills. You must also be over the age of 16.</span></p>					</div>
						</div>
				</div>
						</div>
					</div>
		</div>
								</div>
					</div>
		</section>
									</div>
			</div>
					</div><div>
				<h3>Course Content</h3>

<div id="course_curriculum">
<table width="100%">				<tbody><tr>
					<td colspan="4">Essentials of European Medical Device Regulations</td>
				</tr>
								<tr>
					<td colspan="4">Module 1: Overview to European Regulations on Medical Devices	</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Overview to European Regulations on Medical Devices</td>
					<td> </td>
					<td><span><i></i> 00:45:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 2: Essential Components of EU MDR	</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Essential Components of EU MDR</td>
					<td> </td>
					<td><span><i></i> 00:42:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 3: Reporting Requirements and Identification	</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Reporting Requirements and Identification</td>
					<td> </td>
					<td><span><i></i> 00:29:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 4: Quality System in Medical Device Regulation	</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Quality System in Medical Device Regulation</td>
					<td> </td>
					<td><span><i></i> 00:38:00</span></td>
				</tr>
				</tbody></table></div>

			</div>
			<h2>Frequently Asked Questions</h2>
                        <div>
                            <div>
                                <span>
                                    Are there any prerequisites for taking the course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        There are no specific prerequisites for this course, nor
                                        are there any formal entry requirements. All you need is
                                        an internet connection, a good understanding of English
                                        and a passion for learning for this course.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    Can I access the course at any time, or is there a set
                                    schedule?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        You have the flexibility to access the course at any time
                                        that suits your schedule. Our courses are self-paced,
                                        allowing you to study at your own pace and convenience.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    How long will I have access to the course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        For this course, you will have access to the course
                                        materials for 1 year only. This means you can review the
                                        content as often as you like within the year, even after
                                        you've completed the course. However, if you buy Lifetime
                                        Access for the course, you will be able to access the
                                        course for a lifetime.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    Is there a certificate of completion provided after
                                    completing the course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        Yes, upon successfully completing the course, you will
                                        receive a certificate of completion. This certificate can
                                        be a valuable addition to your professional portfolio and
                                        can be shared on your various social networks.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    Can I switch courses or get a refund if I'm not satisfied
                                    with the course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        We want you to have a positive learning experience. If
                                        you're not satisfied with the course, you can request a
                                        course transfer or refund within 14 days of the initial
                                        purchase.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    How do I track my progress in the course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        Our platform provides tracking tools and progress
                                        indicators for each course. You can monitor your progress,
                                        completed lessons, and assessments through your learner
                                        dashboard for the course.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    What if I have technical issues or difficulties with the
                                    course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        If you encounter technical issues or content-related
                                        difficulties with the course, our support team is
                                        available to assist you. You can reach out to them for
                                        prompt resolution.
                                    </p>
                                </div>
                            </div>
                        </div>

Janets

Essentials of European Medical Device Regulations

<p><span>The Laboratory Technician is a wonderful learning opportunity for anyone who has a passion for this topic and is interested in enjoying a long career in the relevant industry. It's also for anyone who is already working in this field and looking to brush up their knowledge and boost their career with a recognised certification.     </span></p>
<p><span>This Laboratory Technician consists of several modules that take around 2 hours to complete. The course is accompanied by instructional videos, helpful illustrations, how-to instructions and advice.</span></p>
<p><span>The course is offered online at a very affordable price. That gives you the ability to study at your own pace in the comfort of your home. You can access the modules from anywhere and from any device.</span></p>
<h3><b>Why choose this course</b></h3>
<ul>
<li><span>Earn an</span><span> e-certificate upon successful completion.</span></li>
<li><span>Accessible, informative modules taught by expert instructors</span></li>
<li><span>Study in your own time, at your own pace, through your computer tablet or mobile device</span></li>
<li><span>Benefit from instant feedback through mock exams and multiple-choice assessments</span></li>
<li><span>Get 24/7 help or advice from our email and live chat teams</span></li>
<li><span>Full Tutor Support on Weekdays</span></li>
</ul>
<h3><b>Course Design</b></h3>
<p><span>The course is delivered through our online learning platform, accessible through any internet-connected device. There are no formal deadlines or teaching schedules, meaning you are free to study the course at your own pace.</span></p>
<p><span>You are taught through a combination of</span></p>
<ul>
<li><span>Video lessons</span></li>
<li><span>Online study materials</span></li>
<li><span>Mock exams</span></li>
<li><span>Multiple-choice assessment</span></li>
</ul>
<h3><b>Certification</b></h3>
<div id="course-home">
<div>
<div id="course-home">
<div>
<p>Upon successful completion of the course, you will be able to obtain your course completion PDF Certificate at £9.99. Print copy by post is also available at an additional cost of £15.99 and the same for PDF and printed transcripts.</p>
</div>
</div>
</div>
</div><div>
				<h3>Course Content</h3>

<div id="course_curriculum">
<table width="100%">				<tbody><tr>
					<td colspan="4">Module 01: Introduction to Laboratory Technician</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 01: Introduction to Laboratory Technician</td>
					<td> </td>
					<td><span><i></i> 00:10:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 02: Role, Rules and Policies of Medical Laboratory Services</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 02: Role, Rules and Policies of Medical Laboratory Services</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 03: Laboratory Equipments</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 03: Laboratory Equipments</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 04: How to Work with Microscope</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 04: How to Work with Microscope</td>
					<td> </td>
					<td><span><i></i> 00:10:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 05: Solutions Used in Medical Laboratory</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 05: Solutions Used in Medical Laboratory</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 06: Sterilisation and Disinfection</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 06: Sterilisation and Disinfection</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 07: How to Decontaminate Reusable Medical Devices</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 07: How to Decontaminate Reusable Medical Devices</td>
					<td> </td>
					<td><span><i></i> 00:20:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 08: Laboratory Accidents and Safety</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 08: Laboratory Accidents and Safety</td>
					<td> </td>
					<td><span><i></i> 00:15:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 09: Quality Assurance</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 09: Quality Assurance</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 10: Standard Operating Procedures</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 10: Standard Operating Procedures</td>
					<td> </td>
					<td><span><i></i> 00:10:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 11: Glossary</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Module 11: Glossary</td>
					<td> </td>
					<td><span><i></i> 00:05:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Order your Certificates &amp; Transcripts	</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Order your Certificates &amp; Transcripts</td>
					<td> </td>
					<td><span><i></i> 00:00:00</span></td>
				</tr>
				</tbody></table></div>

			</div>
			<h2>Frequently Asked Questions</h2>
                        <div>
                            <div>
                                <span>
                                    Are there any prerequisites for taking the course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        There are no specific prerequisites for this course, nor
                                        are there any formal entry requirements. All you need is
                                        an internet connection, a good understanding of English
                                        and a passion for learning for this course.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    Can I access the course at any time, or is there a set
                                    schedule?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        You have the flexibility to access the course at any time
                                        that suits your schedule. Our courses are self-paced,
                                        allowing you to study at your own pace and convenience.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    How long will I have access to the course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        For this course, you will have access to the course
                                        materials for 1 year only. This means you can review the
                                        content as often as you like within the year, even after
                                        you've completed the course. However, if you buy Lifetime
                                        Access for the course, you will be able to access the
                                        course for a lifetime.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    Is there a certificate of completion provided after
                                    completing the course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        Yes, upon successfully completing the course, you will
                                        receive a certificate of completion. This certificate can
                                        be a valuable addition to your professional portfolio and
                                        can be shared on your various social networks.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    Can I switch courses or get a refund if I'm not satisfied
                                    with the course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        We want you to have a positive learning experience. If
                                        you're not satisfied with the course, you can request a
                                        course transfer or refund within 14 days of the initial
                                        purchase.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    How do I track my progress in the course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        Our platform provides tracking tools and progress
                                        indicators for each course. You can monitor your progress,
                                        completed lessons, and assessments through your learner
                                        dashboard for the course.
                                    </p>
                                </div>
                            </div>
                        </div>
                        
                        <div>
                            <div>
                                <span>
                                    What if I have technical issues or difficulties with the
                                    course?
                                </span>
                                <div>
                                    <span></span>
                                </div>
                            </div>
                            <div>
                                <div>
                                    <p>
                                        If you encounter technical issues or content-related
                                        difficulties with the course, our support team is
                                        available to assist you. You can reach out to them for
                                        prompt resolution.
                                    </p>
                                </div>
                            </div>
                        </div>

Medical Laboratory

Lab Technician

Laboratory

Laboratory Technician

Anatomical Pathology Technician

Getreskilled (UK)

Pharmaceutical

Take our part-time online “Conversion Course into Pharmaceutical Manufacturing“
NO Previous Industry Experience or Science Qualifications Required

Retrain ONLINE for a Higher-Paying Job in the Pharma Manufacturing Industry in 10-Weeks

Full Price

1/4 Monthly Instalments

<div id="course-pills-1">Duration<p>3 Days</p><p>18 CPD hours</p>This course is intended for<p>CliniciansUniversitiesHospitalsHealthcare ExecutivesEntrepreneursInvestors</p>Overview<p>Intro to blockchainMajor healthcare use cases of blockchainUnderstand different use cases of PEB that have already been implemented and encourage thought of new potential use cases.</p><p>This course covers the intersection of healthcare and Blockchain.   Training will include an overview of Blockchain, and uses for Blockchain in the healthcare industry, from medical records, to medical devices, insurance and more.</p></div><div id="course-pills-2"><h4>Day 1</h4><ul><li>History of blockchain</li><li>Blockchain 101</li><li>Decentralization/centralization</li><li>Distributed ledger-private vs public</li><li>Mining and consensus mechanisms</li><li>Intro to healthcare on blockchain including Medical records FHIR, HL7</li></ul><h4>Day 2</h4><ul><li>Patient identity</li><li>Value-based care and concepts (discuss outcome-based smart contracts)</li><li>Medical devices, Wearables, IoT </li><li>Patient adherence monitoring (with tokenized incentives-could also discuss with pt. empowerment), incentives, etc.</li><li>Interoperability and other obstacles of implementation (industry inertia, large data sets, inherent resistance to change)</li></ul><h4>Day 3</h4><ul><li>Supply chain (substandard and falsified medicines, divergence, compliance with DSCSA)</li><li>Logistics</li><li>Insurance (eligibility, reduced overhead, claims processing)</li><li>Data sets</li><li>AI technology (theoretical use cases)</li><li>PT empowerment 1 &amp; 2 (digital health wallet with access driven by smart contracts, monetizing data for sharing)</li></ul></div><div id="course-pills-3"><h4>Additional course details:</h4><br /><p>Nexus Humans Blockchain for Healthcare Professionals training program is a workshop that presents an invigorating mix of sessions, lessons, and masterclasses meticulously crafted to propel your learning expedition forward. </p><p></p> This immersive bootcamp-style experience boasts interactive lectures, hands-on labs, and collaborative hackathons, all strategically designed to fortify fundamental concepts. <p></p>Guided by seasoned coaches, each session offers priceless insights and practical skills crucial for honing your expertise. Whether you're stepping into the realm of professional skills or a seasoned professional, this comprehensive course ensures you're equipped with the knowledge and prowess necessary for success.  <p></p>While we feel this is the best course for the Blockchain for Healthcare Professionals course and one of our Top 10 we encourage you to read the course outline to make sure it is the right content for you.  <p></p>Additionally, private sessions, closed classes or dedicated events are available both live online and at our training centres in Dublin and London, as well as at your offices anywhere in the UK, Ireland or across EMEA.<p></p></div>

Nexus Human

Healthcare IT

Cryptocurrency & Blockchain

Health Coach Training

Healthcare Marketing

Healthcare

Blockchain for Healthcare Professionals

<p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" id="isPasted" fr-original-style=" color: rgb(51, 51, 51);">This module provides an introduction to the basics of medical device regulation, especially the requirements that manufacturers must meet in order to market devices in Europe and the USA.</p><p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(51, 51, 51);">We explain what medical devices are and give examples of the various types. We outline the principles of their regulation and the criteria for placing them on the market. We identify major players in regulation worldwide.</p><p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(51, 51, 51);">We then outline prominent characteristics of the regulation of medical devices in the USA and in Europe. The module is up to date with the current upheaval in European Union legislation on medical devices.</p>

Zenosis

Good Manufacturing Practice (GMP)

Biotechnology

Pharmacology

Drug Safety

Medical

This module provides an introduction to the basics of medical device regulation, especially the requirements that manufacturers must meet in order to market devices in Europe and the USA.

MD01: An Introduction to the Regulation of Medical Devices

<div>
                        
                        <div>
                            <p> </p>
<p>During this training course, you will also gain a thorough understanding of the best practices of Medical Devices Quality Management Systems and be able to improve an organization`s overall performance by consistently providing safe and qualitative medical devices.</p>
<p>After mastering all the necessary concepts of Medical Devices Quality Management Systems, you can sit for the exam and gain the "Certified ISO 13485 Lead Implementer' Certificate. By holding this Certificate, you will be able to demonstrate that you have the practical knowledge and professional capabilities to implement ISO 13485 in an organization. </p>
                        </div>
                    </div>
                    <div>
                        <h2>About This Course</h2>
                        <div>
                            <p> </p>
<p>Learning Objectives</p>
<ul>
<li>Acknowledge the correlation between ISO 13485 and other standards and regulatory frameworks </li>
<li>Master the concepts, approaches, methods and techniques used for the implementation and effective management of a MDQMS</li>
<li>Learn how to interpret the ISO 13485 requirements in the specific context of an organization</li>
<li>Learn how to support an organization to effectively plan, implement, manage, monitor and maintain a MDQMS</li>
<li>Acquire the expertise to advise an organization in implementing Medical Devices Quality Management System best practices</li>
</ul>
<p> </p>
<p>Course Agenda</p>
<ul>
<li><span><strong>Day 1</strong>:</span> Introduction to ISO 13485 and initiation of a MDQMS</li>
<li><span><strong>Day 2</strong>:</span> Plan the implementation of a MDQMS</li>
<li><span><strong>Day 3</strong>:</span> Implementation of a MDQMS</li>
<li><strong>Day 4:</strong> MDQMS monitoring, measurement, continuous improvement and preparation for a certification audit, and the final exam.</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Assessment</h2>
                        <div>
                            <p> </p>
<p> </p>
<p>Delegates sit a combined exam, consisting of in-course quizzes and exercises, as well as a final 12 question, essay type exam on Day 4 of the course. The overall passing score is 70%, to be achieved within the 150 minute time allowance.</p>
<p>Exam results are provided within 24 hours, with both a Certificate and a digital badge provided as proof of success.</p>
                        </div>
                    </div>
                    <div>
                        <h2>Prerequisites</h2>
                        <div>
                            <p> </p>
<p><span>A fundamental understanding of ISO 13485 and comprehensive knowledge of implementation principles.</span></p>
                        </div>
                    </div>
                    <div>
                        <h2>What's Included?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Certification fees are included on the exam price</li>
<li>Training material containing over 450 pages of information and practical examples will be distributed</li>
<li>An attestation of course completion worth 32 CPD (Continuing Professional Development) credits will be issued to the participants who have attended the training course.</li>
<li>In case of exam failure, you can retake the exam within 12 months for free</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Who Should Attend?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Managers or consultants involved in Medical Devices Quality Management</li>
<li>Expert advisors seeking to master the implementation of a Medical Devices Quality Management System</li>
<li>Individuals responsible for maintaining conformance with MDQMS requirements</li>
<li>MDQMS team members</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Accreditation</h2>
                        <div>
                            <p><img src="https://www.the-training-centre.com/content/img/National%20Accreditation%20Service%20(3).jpg" height="201" width="258" /></p>
                        </div>
                    </div>
                    <div>
                        <h2>Provided by</h2>
                        <div>
                            <p> </p>
<p>This course is Accredited by <a title="NACS" href="http://www.nacs.ee" target="_blank">NACS</a> and Administered by the <a title="IECB" href="https://www.iecb.org" target="_blank">IECB</a></p>
                        </div>
                    </div>

Training Centre

ISO 13485 Lead Implementer

<div>
                        
                        <div>
                            <p> </p>
<p><span>ISO 13485 Foundation training enables you to learn the basic elements to implement and manage a Medical Devices Quality Management System (MDQMS) as specified in ISO 13485. During this training course, you will be able to understand the different modules of a MDQMS, including MDQMS policy, procedures, performance measurements, management commitment, internal audit, management review and continual improvement.</span></p>
<p><span><span>After completing this course, you can sit for the exam and gain "Certified ISO 13485 Foundation' Certification. This Certificate shows that you have understood the fundamental methodologies, requirements, framework and management approach. </span></span></p>
                        </div>
                    </div>
                    <div>
                        <h2>About This Course</h2>
                        <div>
                            <p> </p>
<p>Learning Objectives</p>
<ul>
<li>Understand the elements and operations of a Medical Devices Quality Management System (MDQMS)</li>
<li>Acknowledge the correlation between ISO 13485 and other standards and regulatory frameworks</li>
<li>Understand the approaches, methods and techniques used for the implementation and  management of a MDQMS</li>
</ul>
<p> </p>
<p>Course Agenda</p>
<ul>
<li>
<p><span>Day 1</span>: Introduction to Medical Devices Quality Management System (MDQMS) concepts as required by ISO 13485</p>
</li>
<li>
<p>Day 2: Medical Devices Quality Management System requirements and Certification Exam  </p>
</li>
</ul>
<p> </p>
                        </div>
                    </div>
                    <div>
                        <h2>Assessment</h2>
                        <div>
                            <p> </p>
<p> </p>
<p>Delegates sit a combined exam, consisting of in-course quizzes and exercises, as well as a final 40 question, multiple choice exam on Day 2 of the course. The overall passing score is 70%, to be achieved within the 60 minute time allowance.</p>
<p>Exam results are provided within 24 hours, with both a Certificate and a digital badge provided as proof of success.</p>
<p> </p>
                        </div>
                    </div>
                    <div>
                        <h2>Prerequisites</h2>
                        <div>
                            <p> </p>
<p><span>None</span></p>
                        </div>
                    </div>
                    <div>
                        <h2>What's Included?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Certification fees are included on the exam price</li>
<li>Training material containing over 200 pages of information and practical examples will be distributed</li>
<li>An attestation of course completion worth 14 CPD (Continuing Professional Development) credits will be issued to the participants who have attended the training course.</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Who Should Attend?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Individuals involved in Medical Devices Quality Management</li>
<li>Individuals seeking to gain knowledge about the main processes of Medical Devices Quality Management Systems (MDQMS)</li>
<li>Individuals interested to pursue a career in Medical Devices Quality Management</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Accreditation</h2>
                        <div>
                            <p><img src="https://www.the-training-centre.com/content/img/National%20Accreditation%20Service%20(3).jpg" height="201" width="258" /></p>
                        </div>
                    </div>
                    <div>
                        <h2>Provided by</h2>
                        <div>
                            <p> </p>
<p>This course is Accredited by <a title="NACS" href="http://www.nacs.ee" target="_blank">NACS</a> and Administered by the <a title="IECB" href="https://www.iecb.org" target="_blank">IECB</a></p>
                        </div>
                    </div>

ISO 13485 Quality Management Foundation

<div>
                        
                        <div>
                            <p> </p>
<p>During this training course, delegates will acquire the knowledge and skills to plan and carry out internal and external audits in compliance with ISO 19011 and ISO/IEC 17021-1 certification process.</p>
<p>Based on practical exercises, you will learn audit techniques and become competent to manage an audit program, audit team, communication with customers, and understand reporting requirements.</p>
<p>After acquiring the necessary expertise to perform this audit, you can sit for the exam and gain the "Certified ISO 13485 Lead Auditor' Certificate. By holding this Certificate, delegates can demonstrate that they have the competencies to audit organizations based on best practices.</p>
                        </div>
                    </div>
                    <div>
                        <h2>About This Course</h2>
                        <div>
                            <p> </p>
<p><strong>Learning Outcomes</strong></p>
<p> </p>
<ul>
<li>Review a Medical Devices Quality Management System based on ISO 13485</li>
<li>Acknowledge the correlation between ISO 13485 and other standards and regulatory frameworks</li>
<li>Understand an auditor's role to: plan, lead and follow-up on a management system audit in accordance with ISO 19011</li>
<li>Learn how to lead an audit and audit team</li>
<li>Learn how to interpret the requirements of ISO 13485 in the context of a MDQMS audit</li>
<li>Acquire the competencies of an auditor to: plan an audit, lead an audit, draft reports, and follow-up on an audit in compliance with ISO 19011</li>
</ul>
<p> </p>
<p>Course Agenda</p>
<p> </p>
<ul>
<li><span><strong>Day 1</strong>:</span> Introduction to Medical Devices Quality Management Systems (MDQMS) and ISO 13485</li>
<li><span><strong>Day 2</strong>:</span> Audit principles, preparation and launching of an audit</li>
<li><span><strong>Day 3</strong>:</span> On-site audit activities </li>
<li><span><strong>Day 4</strong>: </span>Closing the audit and final exam.</li>
</ul>
<p> </p>
                        </div>
                    </div>
                    <div>
                        <h2>Assessment</h2>
                        <div>
                            <p> </p>
<p> </p>
<p>Delegates sit a combined exam, consisting of in-course quizzes and exercises, as well as a final essay style exam, consisting of 12 questions, on Day 4 of the course. The overall passing score is 70%, to be achieved within the 150 minute time allowance.</p>
<p>Exam results are provided within 24 hours, with both a Certificate and a digital badge provided as proof of success.</p>
<p> </p>
                        </div>
                    </div>
                    <div>
                        <h2>Prerequisites</h2>
                        <div>
                            <p> </p>
<p><span>An understanding of ISO 13485 requirements and knowledge of audit principles.</span></p>
                        </div>
                    </div>
                    <div>
                        <h2>What's Included?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Certification fees are included on the exam price</li>
<li>Training material containing over 500 pages of information and practical examples will be distributed</li>
<li>An attestation of course completion worth 32 CPD (Continuing Professional Development) credits will be issued to the participants who have attended the training course.</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Who Should Attend?</h2>
                        <div>
                            <p> </p>
<ul>
<li>Auditors seeking to perform Medical Devices Quality Management System (MDQMS) certification audits </li>
<li>Managers or consultants seeking to understand the Medical Devices Quality Management System audit requirements</li>
<li>Individuals responsible for maintaining conformance with Medical Devices Quality Management System requirements</li>
</ul>
                        </div>
                    </div>
                    <div>
                        <h2>Accreditation</h2>
                        <div>
                            <p><img src="https://www.the-training-centre.com/content/img/National%20Accreditation%20Service%20(3).jpg" height="201" width="258" /></p>
                        </div>
                    </div>
                    <div>
                        <h2>Provided by</h2>
                        <div>
                            <p> </p>
<p>This course is Accredited by <a title="NACS" href="http://www.nacs.ee" target="_blank">NACS</a> and Administered by the <a title="IECB" href="https://www.iecb.org" target="_blank">IECB</a></p>
                        </div>
                    </div>

ISO 13485 Lead Auditor

<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
					<div>
			<div></div>
		</div>
				</div>
				</div>
				<div>
				<div>
			
				</div>
				<div>
				<div>
					<div><p>The Essentials of European Medical Device Regulations course provides a comprehensive overview of the EU MDR, covering everything from classification and reporting to quality systems. You'll learn from experienced professionals and gain the knowledge and skills to successfully ensure your devices comply with the latest regulations and bring them to market.</p><p>In the first section, you will explore the European Medical Device Regulations (EU MDR). Picture yourself gaining a bird's-eye view of the regulatory framework governing European medical devices. As you delve into the essential components of EU MDR in Section 02, envision yourself gaining a profound understanding of device classification, conformity assessment procedures, and the intricacies of clinical evaluations. It's a voyage of discovery that lays the foundation for your expertise.</p><p>Now, picture yourself in Section 03, where you dive into the depths of reporting requirements and identification. You'll acquire the knowledge and confidence to navigate adverse event reporting and product seamlessly recalls. Finally, in Section 04, envision yourself immersed in the world of quality systems within medical device regulation. Gain the skills to ensure product safety and efficacy while adhering to the highest industry standards.</p><p>By completing this course, you'll emerge as a knowledgeable and adept professional ready to conquer the challenges of European Medical Device Regulations. Whether you're a seasoned industry expert seeking to sharpen your skills or a newcomer eager to embark on a rewarding healthcare career, this course is your gateway to success. Join us on this captivating journey and become a master of European medical device compliance.</p><p>Are you ready to embark on a transformative journey through the intricacies of European Medical Device Regulations? Enroll today and unlock the secrets to compliance, quality, and success in the healthcare industry.</p></div>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</div></section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2><b> Learning outcome</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Master the fundamentals of European Medical Device Regulations.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Understand the key components of EU MDR, including classification and conformity assessment.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Learn how to navigate reporting requirements and handle identification in compliance with regulations.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Gain proficiency in quality systems integral to medical device regulation.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Acquire the skills needed to ensure product safety and efficacy.</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
					</div>
				</div>
				<div>
				<div>
					
			</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Why should I take this course?</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Gain a comprehensive understanding of the EU MDR and its requirements</span>
									</li>
								<li>
											<span>
													</span>
										<span>Learn from experienced professionals who have helped companies comply with the EU MDR</span>
									</li>
								<li>
											<span>
													</span>
										<span>Get the knowledge and skills you need to ensure your devices comply with the latest regulations and bring them to market successfully</span>
									</li>
								<li>
											<span>
													</span>
										<span>Stay ahead of the curve and avoid costly mistakes</span>
									</li>
								<li>
											<span>
													</span>
										<span>Protect the safety and well-being of your patients</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Career Path</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Regulatory Affairs Specialist</span>
									</li>
								<li>
											<span>
													</span>
										<span>Quality Assurance Manager</span>
									</li>
								<li>
											<span>
													</span>
										<span>Medical Device Consultant</span>
									</li>
								<li>
											<span>
													</span>
										<span>Clinical Research Associate</span>
									</li>
								<li>
											<span>
													</span>
										<span>Compliance Analyst</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section>
				<section>
						<div>
				<div>
				<div>
			<div>
					<div>
				<div>
				<div>
			<h2> <b>Requirements</b></h2>		</div>
				</div>
				<div>
				<div>
					<ul>
							<li>
											<span>
													</span>
										<span>Basic knowledge of medical devices and healthcare regulations.</span>
									</li>
								<li>
											<span>
													</span>
										<span>Access to a computer with internet connectivity.</span>
									</li>
								<li>
											<span>
													</span>
										<span>A desire to excel in the field of medical device regulation.</span>
									</li>
						</ul>
				</div>
				</div>
						</div>
			</div>
		</div>
						</div>
			</div>
		</section><div>
                            <div>
                                <h2>Course Curriculum</h2>
                            </div>
                            			<div>
				

<div>
<table width="100%">				<tbody><tr>
					<td colspan="4"><strong>Section 01: Overview to European Regulations on Medical Devices</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Overview to European Regulations on Medical Devices</td><td><span>🕐 00:33:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 02: Essential Components of EU MDR</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Essential Components of EU MDR</td><td><span>🕐 00:29:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 03: Reporting Requirements and Identification</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Reporting Requirements and Identification</td><td><span>🕐 00:16:00</span></td>
				</tr>
								<tr>
					<td colspan="4"><strong>Section 04: Quality System in Medical Device Regulation</strong></td>
				</tr>
								<tr>
					<td>▶</td>
					<td>Quality System in Medical Device Regulation</td><td><span>🕐 00:25:00</span></td>
				</tr>
				</tbody></table></div>

			</div>
		                        </div>

Medical Device Development

Master the European Medical Device Regulations (EU MDR) with this comprehensive course. Gain the knowledge and skills you need to comply with the EU MDR and successfully bring your medical devices to market.

<p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" id="isPasted" fr-original-style=" color: rgb(51, 51, 51);">Part 11 of Title 21 of the US Code of Federal Regulations (21CFR11) sets out requirements that computer systems must meet to satisfy the Food and Drug Administration (FDA) that electronic records and electronic signatures provided by those systems are trustworthy and reliable to the same extent as paper counterparts. The regulation sets out controls and procedures which need to be established and followed for relevant computer systems in FDA-regulated environments. An FDA-regulated environment is a &lsquo;GxP&rsquo; environment operated by an organisation involved in activities leading to the marketing of drugs or medical devices in the USA; examples are drug manufacturing sites, medical device manufacturing sites, analytical laboratories, clinical investigational sites, and nonclinical study laboratories.</p><p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(51, 51, 51);">21CFR11 applies to records that are required to be submitted to the FDA, or that are subject to FDA inspection, and that are in electronic form &ndash; that is, as computer files. It applies to all computer systems used to create, modify, maintain, archive, retrieve, or transmit such records &ndash; from a humble spreadsheet program to a complex information management system.</p><p style="color: rgb(51, 51, 51); font-size: var(--font-size); box-sizing: border-box;" fr-original-style=" color: rgb(51, 51, 51);">Companies that market or intend to apply for approval to market drugs or medical devices in the USA must comply with 21CFR11, whether or not they are based in the USA. Suppliers to such companies of materials, equipment, or data that are subject to FDA regulation must also comply.</p>

21CFR11 applies to records that are required to be submitted to the FDA, or that are subject to FDA inspection, and that are in electronic form – that is, as computer files. It applies to all computer systems used to create, modify, maintain, archive, retrieve, or transmit such records – from a humble spreadsheet program to a complex information management system.

ICT01: Compliance with Regulation 21 CFR Part 11 on Electronic Records and Electronic Signatures

<p>Learn the recent EU medical device regulations and alterations and turn yourself into an asset for the health &amp; care job sector. The starting salary of a medical device consultant is at least £35k annually. So, why wait? Just take the course.</p><p>The Medical Device Regulations (EU) course will help you understand the basic requirements and ideas of the European Medical Devices Regulation. This course will walk you through the important elements of EU MDR, including regulatory developments in the European market, the structure of the regulation, and the partners affected by it. It contains critical information on reporting requirements and identification, as well as an overview of the UK Good Manufacturing Practice Guides.</p><p>Therefore, enrol in our Medical Device Regulations (EU) course to enlarge your knowledge and grab the opportunities that are waiting for you in the near future.</p><p><strong>At the end of the course, learners will be able to:</strong></p><ul><li>Learn more about the EU Medical Devices Regulations and their potential applications</li><li>Discover the most recent alterations to the European market's regulations</li><li>Recognise what EU MDR actually implies in practice</li><li>Possess a thorough understanding of identification and reporting requirements</li><li>Learn in-depth information on how the new rules affect producers, importers, distributors, and EU representatives of medical devices</li><li>Recognise the full procedure for CE marking in accordance with the Medical Devices Regulation (MDR)</li></ul><p><strong>Expert Support</strong></p><p>Dedicated tutor support and 24/7 customer support are available to all students with this premium quality course.</p><p><strong>Key Benefits</strong></p><ul><li>Learning materials of the Design course contain engaging voiceover and visual elements for your comfort.</li><li>Get 24/7 access to all content for a full year.</li><li>Each of our students gets full tutor support on weekdays (Monday to Friday)</li></ul><p><strong>Please note</strong>: This course only gives you the theoretical knowledge that you need to excel in this field. This Essentials of European Medical Device Regulations course doesn't entitle you to practise as a professional in this specific field.</p><p><strong>COURSE CURRICULUM</strong></p><p><strong>Essentials of European Medical Device Regulations</strong></p><ul><li>Module 1: Overview to European Regulations on Medical Devices</li><li>Module 2: Essential Components of EU MDR</li><li>Module 3: Reporting Requirements and Identification</li><li>Module 4: Quality System in Medical Device Regulation</li></ul><p><strong>Meet the Accreditation</strong></p><p><strong>The CPD Certification Service (CPD UK</strong>) assures the <strong>Essentials of European Medical Device Regulations</strong> course training and learning activities are relevant, reliable, and upto date.</p><p><strong>Course Assessment </strong></p><p>To simplify the procedure of evaluation and accreditation for learners, we provide an automated assessment system. Upon completion of an online module, you will immediately be given access to a specifically crafted MCQ test. The results will be evaluated instantly, and the score will be displayed for your perusal. For each test, the pass mark will be set to 60%.</p><p>When all tests have been successfully passed, you will be able to order a certificate endorsed by the Quality Licence Scheme.</p><p><strong>Exam &amp; Retakes:</strong></p><p>It is to inform our learners that the initial exam for this online course is provided at no additional cost. In the event of needing a retake, a nominal fee of £9.99 will be applicable.</p><p><strong>Certification</strong></p><p>Upon successful completion of the assessment procedure, learners can obtain their certification by placing an order and remitting a fee of £9 for PDF Certificate and £15 for the Hardcopy Certificate within the UK ( An additional £10 postal charge will be applicable for international delivery).</p><h2>
        
        <div>CPD</div>
    </h2>

                        <div id="cpd">
                            <div>
                                <div>
                                    <div>
                                        10 CPD hours / points
                                    </div>
                                        <div>
                                            Accredited by The CPD Certification Service
                                        </div>
                                </div>
                            </div>
                        </div><h2>
        
        <div>Who is this course for?</div>
    </h2>

                        <div id="who_is_this_course_for">
                            <ul><li>Senior Regulatory Affairs Specialist</li><li>Sales Representative CP</li><li>Medical Writer</li><li>Quality System Engineer</li></ul>
                        </div><h2>
        
        <div>Requirements</div>
    </h2>

                        <div id="requirements">
                            <p>This Medical Device Regulations (EU) course is open to all, with no formal entry requirements.</p>
                        </div><h2>
        
        <div>Career path</div>
    </h2>

                        <div id="career_path">
                            <ul><li>Medical Secretary (£17,500 to £24,000) per annum</li><li>Medical illustrator (£25,654 to £39,026) per annum</li><li>Regulatory Medical Device Engineer (£50,000 to £60,000) per annum</li><li>Regulatory Medical Device Consultant (£50,000 to £60,000) per annum</li><li>Midwife - Medical Device Trainer (£35,000 to £45,000) per annum</li></ul>
                        </div>

Medical Device Regulations (EU) Course

<div id="course-pricing" fr-original-style="" style="box-sizing: border-box;">
          </div><p id="isPasted" fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Explore the intricacies of European Medical Device Regulations (EU MDR) with our comprehensive course.&nbsp;</span></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Gain a solid understanding of the European regulations governing medical devices, including the essential components of EU MDR. Learn about reporting requirements, identification processes, and the quality system involved in regulating medical devices.</span></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Throughout the course, you&#39;ll grasp the significance of adhering to regulatory standards and guidelines for medical devices. With expert guidance and accessible online materials, this course provides a great learning experience for individuals from any academic background.&nbsp;</span></p><p fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">Upon completion, receive a CPD certificate to validate your knowledge and enhance your career prospects in regulatory affairs, quality assurance, compliance, and more.</span></p><h2 dir="ltr" id="isPasted" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Learning Outcome of EU Medical Device Regulations</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li id="isPasted" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Learn the overview of European regulations governing medical devices.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Gain insight into the essential components of EU Medical Device Regulations (MDR).</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Understand the reporting requirements and identification processes related to medical devices.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Acquire knowledge about the quality system involved in regulating medical devices.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Learn about compliance with EU MDR standards and guidelines.</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Understand the importance of adhering to regulatory requirements for medical devices.</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Key Features of the Course</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">A CPD certificate that is recognised worldwide.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">A great online learning experience.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Interesting and unique online materials and activities.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Expert guidance and support from the field leaders.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Access to the study resources anytime you want.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Friendly and helpful customer service and admin support by email, phone, and chat from Monday through Friday.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Get a year-long access to the course.</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Requirements</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">No prerequisites; suitable for individuals from any academic background.</li><li dir="ltr" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Accessible course materials from any internet-enabled device.</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">CPD Certificate from Course Gate</span></h2><p dir="ltr" fr-original-style="" style="color: var(--text); font-size: var(--font-size); box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">At the successful completion of the course, you can obtain your CPD certificate from us. You can order the PDF certificate for &pound;9 and the hard copy for &pound;15. Also, you can order both PDF and hardcopy certificates for &pound;22.</span></p><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Career path</span></h2><ul fr-original-style="" style="box-sizing: border-box;"><li id="isPasted" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Regulatory Affairs Specialist</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Quality Assurance Manager</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Compliance Officer</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Product Safety Manager</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Clinical Affairs Specialist</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Medical Device Consultant</li></ul><h2 dir="ltr" fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color:#000000;">Course Curriculum</span><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);"><br fr-original-style="" style="box-sizing: border-box;"></span></h2><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><section fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><div fr-original-style="" style="box-sizing: border-box;"><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></div><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></div><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></div><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></div><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></section><span style="color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="color: rgb(0, 0, 0);">
</span></div><ul fr-original-style="" style="box-sizing: border-box;"><li id="isPasted" style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 01: Overview to European Regulations on Medical Devices</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 02: Essential Components of EU MDR</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 03: Reporting Requirements and Identification</li><li style="font-size: 16px; color: rgb(0, 0, 0); box-sizing: border-box;" fr-original-style="font-size: 16px; color: rgb(0, 0, 0);">Module 04: Quality System in Medical Device Regulation</li></ul></div>

Course Gate

Explore the essentials of European Medical Device Regulations (EU MDR) with our comprehensive course. Gain insights into regulatory requirements, quality systems, and reporting protocols to ensure compliance in the healthcare industry.

Essentials EU Medical Device Regulations

<p>Do you want to improve your career prospects in Health and Care? One Education brings a range of high-quality Health and Care courses that are ideal for you, whether you're a beginner or aspire for higher roles in research, leadership, and education.</p><p>This <strong>Essentials of European Medical Device Regulations - CPD Certified Course </strong>is excellent for improving your knowledge, skill set and competencies in relevant areas of Health and Care.</p><p><strong>Learning Outcomes of the </strong><strong>Essentials of European Medical Device Regulations - CPD Certified</strong><strong> Training:</strong></p><ul><li>Deepen your understanding of the EU Medical Devices Regulations and how it can be applied</li><li>Learn about recent regulatory changes in the European market</li><li>Understand what EU MDR means in practice</li><li>Have an excellent understanding of reporting requirements and identification</li><li>Gain in-depth knowledge of how the new regulations affect medical device manufacturers, importers, distributors and EU Representatives</li><li>Understand the complete process for CE marking under the Medical Devices Regulation (MDR)</li></ul><p>The course is developed after thorough research and expertise from seasoned professionals. Having prior learning is extremely helpful if you aim to enter the Health and Care sector as a beginner.</p><p>This will be delivered exclusively through our online platform, where you completely control your learning experience. You can go through the modules and study materials at your own pace without any restrictions. And you'll receive a recognised certificate as proof of your newly acquired or improved knowledge and skills.</p><p><strong>Why choose CPD Certification Service Accredited (CPD UK) course?</strong></p><ul><li>World's leading and largest independent CPD accreditation institution</li><li>Pioneering CPD quality standards since 1996</li><li>Over 20 thousand registered CPD Providers and Courses</li><li>With 25 years experience providing industry-leading CPD certification service and support</li></ul><p>Take a step towards reaching your true potential by enrolling in this <strong> Essentials of European Medical Device Regulations - CPD Certified Training</strong>!</p><p>Understand the essential requirements and concepts of the European Medical Devices Regulation, with the Essentials of European Medical Device Regulations course. This course covers the essential components of EU MDR, taking you through regulatory changes in the European market, the structure of the regulation and the partners affected by it. It includes important information on reporting requirements and identification, as we as an overview of the UK Guides to Good Manufacturing Practice.</p><p>Please note: This course only gives you the theoretical knowledge that you need to excel in this field. This Essentials of European Medical Device Regulations doesn't entitle you to practise as a professional in this specific field.</p><p><strong>Course Curriculum:</strong></p><ul><li>Module 1: Overview to European Regulations on Medical Devices</li><li>Module 2: Essential Components of EU MDR</li><li>Module 3: Reporting Requirements and Identification</li><li>Module 4: Quality System in Medical Device Regulation</li></ul><p><strong>Course Assessment</strong></p><p>You will immediately be given access to a specifically crafted MCQ test upon completing an online module. For each test, the pass mark will be set to 60%.</p><p><strong>Exam &amp; Retakes:</strong><br />It is to inform our learners that the initial exam for this online course is provided at no additional cost. In the event of needing a retake, a nominal fee of £9.99 will be applicable.</p><p><strong>Certification</strong><br />Upon successful completion of the assessment procedure, learners can obtain their certification by placing an order and remitting a fee of £9 for PDF Certificate and £15 for the Hardcopy Certificate within the UK ( An additional £10 postal charge will be applicable for international delivery).</p><h2>
        
        <div>CPD</div>
    </h2>

                        <div id="cpd">
                            <div>
                                <div>
                                    <div>
                                        10 CPD hours / points
                                    </div>
                                        <div>
                                            Accredited by The CPD Certification Service
                                        </div>
                                </div>
                            </div>
                        </div><h2>
        
        <div>Who is this course for?</div>
    </h2>

                        <div id="who_is_this_course_for">
                            <p>The <strong>Essentials of European Medical Device Regulations - CPD Certified</strong> training is ideal for highly motivated individuals or teams who want to enhance their professional skills and efficiently skilled employees.</p>
                        </div><h2>
        
        <div>Requirements</div>
    </h2>

                        <div id="requirements">
                            <p>There are no formal entry requirements for the course, with enrollment open to anyone!</p>
                        </div><h2>
        
        <div>Career path</div>
    </h2>

                        <div id="career_path">
                            <p>Learn the essential skills and knowledge you need to excel in your professional life with the help &amp; guidance from our <strong>Essentials of European Medical Device Regulations - CPD Certified</strong> training.</p>
                        </div><h2>
        
        <div>Certificates</div>
    </h2>

                        <div id="optional_extras">
                                    <h4>Certificate of completion</h4>
        <p>
            Digital certificate -
            £9
        </p>
        <h4>Certificate of completion</h4>
        <p>
            Hard copy certificate -
            £15
        </p>
            <div> <p><strong>CPD Certification Service Accredited Certification</strong></p><ul><li>Hardcopy Certificate (within the UK): £15</li><li>Hardcopy Certificate (international): £15 + £10 (postal charge) = £25</li></ul> </div>

                        </div>

Essentials of European Medical Device Regulations - CPD Certified Course

<p>Delve into the intricacies of European medical device regulatory frameworks with our comprehensive course, '<strong>Essentials of European Medical Device Regulations</strong>.' This meticulously structured program provides an in-depth exploration of the critical components and legislative requirements necessary for navigating the complex landscape of medical device regulations in Europe. The first module introduces the foundational aspects of the European regulations, setting the stage for a deeper understanding of the legal and procedural elements that govern this sector. As the course progresses, participants will gain a thorough grasp of the Essential Components of EU MDR (Module 2), the pivotal aspects of Reporting Requirements and Identification (Module 3), and the integral role of Quality Systems in medical device regulation (Module 4). This course is meticulously designed to cater to the needs of professionals seeking a robust understanding of the regulatory environment, ensuring they are well-equipped to adhere to and implement these critical regulations.</p>
<p><strong>Learning Outcomes</strong></p>
<ul>
<li>Acquire a solid foundation in the basic principles and framework of European regulations on medical devices.</li>
<li>Understand the key elements of the EU Medical Device Regulation (MDR) and their application in the industry.</li>
<li>Gain insights into the specific requirements for reporting and identification within the European regulatory context.</li>
<li>Learn about the implementation and management of quality systems in compliance with medical device regulations.</li>
<li>Develop the ability to interpret and apply regulatory guidelines in professional settings, enhancing compliance and operational efficiency.</li>
</ul>
<h3><b>Why choose this Essentials of European Medical Device Regulations<span> course</span>?</b></h3>
<ol>
<li>Unlimited access to the course for a lifetime.</li>
<li>Opportunity to earn a certificate accredited by the <b>CPD Quality Standards</b> and <b>CIQ </b>after completing this course.</li>
<li>Structured lesson planning in line with industry standards.</li>
<li>Immerse yourself in innovative and captivating course materials and activities.</li>
<li>Assessments designed to evaluate advanced cognitive abilities and skill proficiency.</li>
<li>Flexibility to complete the Course at your own pace, on your own schedule.</li>
<li>Receive full tutor support throughout the week, from Monday to Friday, to enhance your learning experience.</li>
<li>Unlock career resources for CV improvement, interview readiness, and job success.</li>
</ol>
<h3><b>Who is this Essentials of European Medical Device Regulations<span> </span></b><b><span>course </span></b><b>for?</b></h3>
<ul>
<li>Professionals in the medical device industry seeking to deepen their understanding of EU regulations.</li>
<li>Regulatory affairs specialists aiming to stay updated with the latest European legislative changes.</li>
<li>Quality assurance personnel in the healthcare sector requiring knowledge of regulatory compliance.</li>
<li>Medical device manufacturers and distributors needing to align their products with EU standards.</li>
<li>Healthcare consultants and advisors focusing on European medical device regulatory frameworks.</li>
</ul>
<h3><b>Career path</b></h3>
<ul>
<li><strong>Regulatory Affairs Manager</strong>: £40,000 - £60,000</li>
<li><strong>Quality Assurance Specialist</strong>: £35,000 - £50,000</li>
<li><strong>Compliance Officer</strong>: £30,000 - £45,000</li>
<li><strong>Product Development Engineer</strong>: £33,000 - £55,000</li>
<li><strong>Healthcare Consultant</strong>: £45,000 - £70,000</li>
<li><strong>Medical Device Auditor</strong>: £37,000 - £53,000</li>
</ul>
<h3><b>Prerequisites</b></h3>
<p><span>This </span><b>Essentials of European Medical Device Regulations</b><span> does not require you to have any prior qualifications or experience. You can just enrol and start learning. This </span><span>course</span><span> was made by professionals and it is compatible with all PC's, Mac's, tablets and smartphones. You will be able to access the course from anywhere at any time as long as you have a good enough internet connection.</span></p>
<h3><b>Certification</b></h3>
<p><span>After studying the course materials, there will be a written assignment test which you can take at the end of the course. After successfully passing the test you will be able to claim the pdf certificate for £4.99 Original Hard Copy certificates need to be ordered at an additional cost of £8.</span></p><div>
				<h3>
	<span>Course Curriculum</span>
</h3>

<div>
<table width="100%">				<tbody><tr>
					<td colspan="4">Module 1: Overview to European Regulations on Medical Devices</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Overview to European Regulations on Medical Devices</td>
					<td> </td>
					<td><span><i></i> 00:43:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 2: Essential Components of EU MDR</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Essential Components of EU MDR</td>
					<td> </td>
					<td><span><i></i> 00:40:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 3: Reporting Requirements and Identification</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Reporting Requirements and Identification</td>
					<td> </td>
					<td><span><i></i> 00:27:00</span></td>
				</tr>
								<tr>
					<td colspan="4">Module 4: Quality System in Medical Device Regulation</td>
				</tr>
								<tr>
					<td><i></i></td>
					<td>Quality System in Medical Device Regulation</td>
					<td> </td>
					<td><span><i></i> 00:36:00</span></td>
				</tr>
				</tbody></table></div>

			</div>

43 Courses delivered Online

Emergency Care Worker Diploma

By Skill Up

European Medical Device Regulations

By Skill Up

Essential Components of European Medical Device Regulations

By Online Training Academy

Sterile services Course

By Elearncollege

Laboratory Technician Diploma at QLS Level 3 Course

By One Education

Linkerd - Service Mesh for Kubernetes

By Packt

Essentials of European Medical Device Regulations

By Janets

Laboratory Technician

By Janets

Retrain ONLINE for a Higher-Paying Job in the Pharma Manufacturing Industry in 10-Weeks

By Getreskilled (UK)

Blockchain for Healthcare Professionals

By Nexus Human