Medical Device Regulations (EU) Course

Description

Learn the recent EU medical device regulations and alterations and turn yourself into an asset for the health & care job sector. The starting salary of a medical device consultant is at least £35k annually. So, why wait? Just take the course.

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.

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.

At the end of the course, learners will be able to:

• Learn more about the EU Medical Devices Regulations and their potential applications
• Discover the most recent alterations to the European market's regulations
• Recognise what EU MDR actually implies in practice
• Possess a thorough understanding of identification and reporting requirements
• Learn in-depth information on how the new rules affect producers, importers, distributors, and EU representatives of medical devices
• Recognise the full procedure for CE marking in accordance with the Medical Devices Regulation (MDR)

Expert Support

Dedicated tutor support and 24/7 customer support are available to all students with this premium quality course.

Key Benefits

• Learning materials of the Design course contain engaging voiceover and visual elements for your comfort.
• Get 24/7 access to all content for a full year.
• Each of our students gets full tutor support on weekdays (Monday to Friday)

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 course doesn't entitle you to practise as a professional in this specific field.

COURSE CURRICULUM

Essentials of European Medical Device Regulations

• Module 1: Overview to European Regulations on Medical Devices
• Module 2: Essential Components of EU MDR
• Module 3: Reporting Requirements and Identification
• Module 4: Quality System in Medical Device Regulation

Meet the Accreditation

The CPD Certification Service (CPD UK) assures the Essentials of European Medical Device Regulations course training and learning activities are relevant, reliable, and upto date.

Course Assessment

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%.

When all tests have been successfully passed, you will be able to order a certificate endorsed by the Quality Licence Scheme.

Exam & Retakes:

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.

Certification

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).

CPD

Who is this course for?

Requirements

Career path