Learning Outcome
- Deepen your understanding of the EU Medical Devices Regulations and how it can be applied
- Learn about recent regulatory changes in the European market
- Understand what EU MDR means in practice
- Have an excellent understanding of reporting requirements and identification
- Gain in-depth knowledge of how the new regulations affect medical device manufacturers, importers, distributors and EU Representatives
- Understand the complete process for CE marking under the Medical Devices Regulation (MDR)
Description
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.
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.
Certification
This course is CPD Certified by The CPD Certification Service. You’ll be eligible to apply for the CPD certified certificate once you complete the course
