3219 Pha courses

The “ISO 17025:2018 Lead Assessor” course provides comprehensive training in Learn how to audit each and every ISO 17025: 2018 and ISO 17011 requirements Learn basic auditing skills; Implement methods to comply with the ISO 17025:2018 requirements. Auditing process and techniques

What Does The Course Include? When choosing a course ensure that it includes both theory and a wide variety of practical content. Every course should include: Anatomy and Physiology Types & structure of the hair Skin, blood and lymphatic circulation Reproductive and endocrine system Theory of Electric Currents Consultations & Record Cards Contra-indications & contra-actions Aftercare advice Choice of needles / probes Accurate probing techniques Legislation, Hygiene and Sterilisation Performing the correct stretch Short-wave Diathermy Galvanic/Blend The Heating Pattern Correct Insertion Techniques The Target Area Unusual Hair Growth FAQ’s Health and Safety Areas Treated This informal and structured weekend will teach all the required techniques necessary to perform successful hair removal treatments. Performed on massage couches, each student will receive guidance on how to effectively perform a full electrolysis treatment on the following areas: Leg Bikini Underarm Nape of Neck Brow Lip Chin Chest The Angel Academy prides itself on always a 100% pass rate for all of its courses since 2003. Classes are kept relatively small so that the tuition can always be of the highest standard. Over the years, all manner of student has come to the Angel Academy from Celebrity to Supermodel to Housewife to Career person looking for a way to relax from the every-day stress and strains that life presents them with.

COURSE OVERVIEW: COPD UPDATE DAY FOR PRIMARY CARE PRACTITIONERS JOIN US FOR A COMPREHENSIVE AND ENRICHING COPD UPDATE DAY, SPECIFICALLY DESIGNED FOR REGISTERED HEALTHCARE PROFESSIONALS WHO ARE CURRENTLY PRACTICING IN THE FIELD OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD). THIS COURSE AIMS TO ENHANCE YOUR EXISTING KNOWLEDGE AND SKILLS, KEEPING YOU UP-TO-DATE WITH THE LATEST DEVELOPMENTS IN COPD MANAGEMENT. DURING THIS INFORMATIVE DAY, YOU WILL DELVE INTO THE ESSENTIALS OF COPD, STARTING FROM ITS FUNDAMENTAL DEFINITION AND DIAGNOSTIC CRITERIA TO THE LATEST INVESTIGATIVE APPROACHES. THE COURSE WILL COVER BOTH NON-PHARMACOLOGICAL AND PHARMACOLOGICAL MANAGEMENT STRATEGIES, WITH A SPECIAL EMPHASIS ON PRACTICAL INHALER TECHNIQUES. WE WILL ALSO EXPLORE THE CURRENT GOLD & NICE GUIDELINES, DISCUSSING THEIR IMPLICATIONS AND PRACTICAL APPLICATIONS IN CLINICAL PRACTICE. A SIGNIFICANT FOCUS WILL BE ON THE MANAGEMENT OF EXACERBATIONS AND LUNG ATTACKS, INCLUDING STRATEGIES FOR PREVENTION AND EFFECTIVE MANAGEMENT TECHNIQUES, WITH A PARTICULAR EMPHASIS ON PATIENT SELF-MANAGEMENT. UNDERSTANDING THE COMPLEXITIES AND CARE REQUIREMENTS OF END-STAGE COPD WILL ALSO BE A KEY ASPECT OF THIS COURSE. THE DAY WILL CONCLUDE WITH INTERACTIVE CASE STUDIES, ALLOWING YOU TO APPLY YOUR REFRESHED KNOWLEDGE IN REAL-WORLD SCENARIOS, ENCOURAGING THE SHARING OF EXPERIENCES AND BEST PRACTICES AMONG YOUR PEERS. THIS COURSE OFFERS A DYNAMIC AND SUPPORTIVE ENVIRONMENT FOR PROFESSIONALS SEEKING TO REFINE THEIR APPROACH TO COPD CARE, COMBINING THEORETICAL LEARNING WITH PRACTICAL APPLICATION LEARNING OUTCOMES: DEFINING AND DIAGNOSING COPD REVIEW AND UPDATE THE DEFINITION AND UNDERSTANDING OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD). REFRESH KNOWLEDGE ON DIAGNOSTIC CRITERIA AND INVESTIGATIONS FOR COPD. NON-PHARMACOLOGICAL MANAGEMENT EXPLORE VARIOUS NON-PHARMACOLOGICAL APPROACHES TO MANAGING COPD. GUIDELINES AND BEST PRACTICES DELVE INTO THE GOLD & NICE GUIDELINES AND THEIR PRACTICAL APPLICATIONS IN COPD MANAGEMENT. PHARMACOLOGY AND INHALER TECHNIQUES UPDATE KNOWLEDGE ON PHARMACOLOGICAL TREATMENTS FOR COPD. MASTER INHALER TECHNIQUES AND UNDERSTAND THEIR CRITICAL ROLE IN COPD MANAGEMENT. LUNG ATTACKS AND EXACERBATION MANAGEMENT LEARN STRATEGIES TO REDUCE THE RISK OF LUNG ATTACKS/EXACERBATIONS. DISCUSS MANAGEMENT TECHNIQUES FOR EXACERBATIONS, INCLUDING PATIENT SELF-MANAGEMENT. MANAGING END-STAGE DISEASE UNDERSTAND THE COMPLEXITIES OF MANAGING END-STAGE COPD. FOCUS ON PALLIATIVE CARE AND IMPROVING QUALITY OF LIFE FOR PATIENTS WITH ADVANCED COPD. CASE STUDIES AND PRACTICAL APPLICATION APPLY KNOWLEDGE THROUGH INTERACTIVE CASE STUDIES. ENCOURAGE SHARING OF EXPERIENCES AND BEST PRACTICES AMONG PARTICIPANTS. This COPD Update Day ensures that seasoned primary care practitioners remain up-to-date with the latest advancements in COPD management, fostering an environment of continuous learning, collaboration, and patient-centered care.

COURSE INFORMATION This highly interactive course will provide guidance on why and how to implement a quality system successfully into the research laboratory. By doing so, you will position your innovation for the success it deserves. But leave things as they are and there is a good chance that your science will not realise its full potential should success, and its consequences, come your way. A quality system in your research laboratory is the most effective and efficient way to: * Help scientists work more efficiently * Ensure discoveries can be defended * Protect the value of intellectual property. This course is particularly aimed at those working in early phase research environments which are not constrained by the regulatory requirements of the Good Practice regulations but are producing intellectual property, testing and/or products for the therapeutic market. For organisational reasons, rather than regulatory ones, this is a place where you need to get it right. The programme is delivered by leaders in the field who, quite simply, ‘have done it’. Whether delegates are at senior management level seeking strategic direction, a laboratory head wishing to deliver science that will stand the test of time or a quality professional thrown in at the deep end, this course will provide key insight and practical guidance to underpin future success. Based on risk based systems, tried and tested over many years in the workplace, the programme will help delegates to define, train, implement and monitor the quality of their research, irrespective of field or discipline. Delegates will learn how to help position their organisation for success. COURSE CONTENT: Delegates will be guided thoughtfully through each key component of the process in a stimulating learning environment. The course probes all avenues of the research quality arena, from an initial understanding of the cultural aspects of the scientific discovery environment, to managing quality in outsourced research programmes. Computer systems and e-data security in the research environment will be discussed and pragmatic solutions described to help manage the ballooning cloud of e-data. In addition, the ever blurring boundary between the regulated and non-regulated research environments will be discussed and delegates given perspective on future developments in the field. With this knowledge, delegates will be able to get it ‘right first time’. IS THIS COURSE FOR YOU? The course is designed for all those involved in the research laboratory quality arena and it has been tailored to meet the needs of scientific management, bench scientists and quality professionals alike. Delegates get immediate access to highly experienced tutors who will share their wisdom and insights in an area where few others have been successful. The course is linked with the RQA guidance which builds on years of experience and forms the foundation of the programme. -------------------------------------------------------------------------------- TUTORS Tutors will be comprised of (click the photos for biographies): LOUISE HANDY Director, Handy Consulting Ltd SANDRINE BONGIOVANNI Associate Director in Research and Quality Compliance, Novartis -------------------------------------------------------------------------------- PROGRAMME Please note timings may be subject to alteration. DAY 1 09:00 REGISTRATION 09:10 WELCOME AND INTRODUCTIONS 09:20 HISTORY AND OVERVIEW OF THE FIELD Examples of business and regulatory risks and the consequences of low quality in research. A look at the standards and guidelines that exist. 10:00 THE CULTURE, THE POLITICS AND THE SCIENTIST'S PERSPECTIVE Understanding research environments, the drivers and the challenges. 10:30 BREAK 10:45 WORKSHOP - RISK MANAGEMENT Thinking about risk management and prioritisation. Looking at the critical factors for the implementations of a successful quality system. 12:15 WORKSHOP - FEEDBACK 12:45 LUNCH 13:45 PERSONNEL, PLANS, PROCEDURES, FACILITIES, EQUIPMENT, MATERIALS AND REAGENTS Looking at planning the work, defining procedures in a way which promotes robust science without compromising brilliance and ensuring that all these elements are demonstrably fit for their intended purpose. 14:30 WORKSHOP - ASSAY VALIDATION How much validation is required at what stage? What do we need to validate an assay? 15:00 WORKSHOP - FEEDBACK 15:15 RESEARCH, WORK RECORDS, ARCHIVES AND RESEARCH REVIEW Data and records which are accurate, attributable, legally attestable and safe to permit reconstruction experiments and studies. Looking at aspects of the work where there is a chance to review, correct or improve the science, the data and the processes. 16:15 CONTINUAL IMPROVEMENT AND QUALITY SYSTEMS Reviewing implementation of a quality system, finding opportunities for improvement, understanding culture change. 16:45 QUESTIONS AND ANSWERS 17:00 CLOSE OF COURSE -------------------------------------------------------------------------------- EXTRA INFORMATION COURSE MATERIAL This course will be run completely online. You will receive an email with a link to our online system, which will house your licensed course materials and access to the remote event. Please note this course will run in UK timezone. THE ADVANTAGES OF THIS INCLUDE:   * Ability for delegates to keep material on a mobile device * Ability to review material at any time pre and post course * Environmental benefits – less paper being used per course Access to an online course group to enhance networking. You will need a stable internet connection, a microphone and a webcam. CPD POINTS 7 Points   DEVELOPMENT LEVEL Develop

The “ISO 20000: 2018 Lead Auditor” course provides comprehensive training in the ISO 20000: 2018 standard and all its requirements from the Lead auditor’s point of view, as well as basic skills necessary to Lead audit activities. It’s a practical-oriented training that should be considered “a must” for every ISO 20000: 2018 Lead auditor. The interactive training program, complete with quizzes, will provide the necessary technical knowledge and understanding of all ISO 20000: 2018 requirements to implement the requirement of the standard and complete ISO 20000: 2018 audit . This ISO Lead auditor training should be taken by individual with interest in conducting internal as well as third part audits according ISO 20000: 2018 standards.

This course is for people who are often the first to respond to a possible medical emergency. This encompasses Police, Firefighters, and medical staff at festivals and events. It also includes Emergency/Community First Responders, Door Supervisors, Close Protection Operatives, and Security Guards. Individuals working in high-risk environments are also catered for. These environments include the military, power stations, agriculture, and manufacturing facilities.

ISO 31000:2018 is an international standard of Risk Management, the existence of it requires competent personnel to interpret its guidelines, address those to integrate Risk Management in an organization’s operations and audit organization to assess the implementation and effectiveness of overall implementation. This course is designed for professionals who are responsible of any aspect of Risk Management as well as for those, specifically, who are pursuing their career in the field of auditing Risk Management. This course enhances the knowledge and skills of delegates to understand the standard and audit it effectively. Course is consisting of study material in form of written details. Attendees of this course will be, on completion, competent to implement Risk Management, Plan, Conduct & Report 1st, 2nd & 3rd party audits. This course also discusses about different risk assessment techniques such as 1. Brainstorming 2. Structured or semi-structured interviews 3. Delphi technique 4. Check-lists 5. Preliminary hazard analysis (PHA) 6. HAZOP 7. Hazard analysis and critical control points (HACCP) 8. Toxicity assessment 9. Structured “What-if” Technique (SWIFT) 10. Scenario analysis 11. Business impact analysis (BIA) 12. Root cause analysis (RCA) 13. Failure modes and effects analysis (FMEA) and failure modes and effects and criticality analysis (FMECA) 14. Fault tree analysis (FTA) 15. Event tree analysis (ETA) 16. Cause-consequence analysis 17. Cause-and-effect analysis 18. Layers of protection analysis (LOPA) 19. Decision tree analysis 20. Human reliability assessment (HRA) 21. Bow tie analysis 22. Reliability centred maintenance 23. Sneak analysis (SA)and sneak circuit analysis (SCI) 24. Markov analysis 25. Monte Carlo simulation 26. Bayesian statistics and Bayes Nets 27. FN curves 28. Risk indices 29. Consequence/ probability matrix 30. Cost/benefit analysis (CBA) 31. Multi-criteria decision analysis (MCDA)   FEATURES OF COUSE ✔ 100% Online Self-paced: Considering the busy lives, we have designed this course to be attended online without bounding with the schedules. To make it interactive, we have created different communication groups where candidate can discuss the points with other fellows as well as the trainers of course. ✔ Testing the Learning: Each section of course is covered with exercise to check your knowledge in real-time, and overall result is affected by exercises you complete. ✔ Self-Scheduling: This 40 Hours full fledge course is designed to match you schedule. You will get a life time access to this course and complete it on your ease. ✔ Superlative Material: The training is designed, developed and reviewed by competent auditors having an extensive experience of auditing in different regions of world. ✔ Approved Course: The course is approved by one of the well-known personal certifying body “IRCP”.   WHO SHOULD ATTEND THIS? This course is recommended to be attended by those who are involved in implementation and/ or auditing of Risk Management System, specifically Risk Managers, Auditors and others willing to add credibility with a widely accepted qualification for auditing. Also, recommended to satisfy the applicable requirement of training and competence, if any. This course can add values to your profile if you are * Intending to perform audits of RM. * A Risk Management Executive/ Management Representative * An Existing Internal Auditor * A Ris Management Consultant * Responsible for implementing the ISO 31000 standard. * Responsibility to evaluate the outcome of internal RM audits and have responsibility/ authority to improve the effectiveness of the RM. * Pursuing to make career in RM auditing.   COURSE DURATION: 40 Learning Hours and extended time of exercise & Exam.   CERTIFICATE: Those who pass all exercises with 50% at least in each exercise and 70% overall marks will be awarded with successfully completion certificate with approval of Exemplar Global and a Lifetime validity.   LANGUAGE OF COURSE: English   PRE-REQUISITES: Knowledge of Risk Management

This course will show delegates how to appraise projects in Excel, incorporate and communicate updates as they happen and ultimately understand how to convert an opportunistic property investment into a core asset that can be sold on.

The “ISO 9001:2015 Lead Auditor” course provides comprehensive training in the ISO 9001:2015 standard and all its requirements from the auditor’s point of view, as well as basic skills necessary to complete an internal audit. It’s a practical-oriented training that should be considered “a must” for every ISO 9001 auditor. This intensive course is specifically designed to train corporate staff to serve as internal ISO 9001 auditors (as required by ISO 9001:2015 ). The interactive training program, complete with quizzes, will provide the necessary technical knowledge and understanding of all ISO 9001:2015 requirements to perform a complete ISO 9001 audit.

CPD accredited Level 3 Effective Auditing & Inspection course. Delivered online (Zoom) by a live tutor. Exam and Certificate fee included in the price.