Overview of EU Regulatory Affairs for Medical Devices Training Course
Module 1 is Free to Attend – Register Below
Learn more about the course (dates, price, skills gained, and when module 1 is) by visiting the course page.
Module 1 Overview | Introduction to Medical Devices and the New MDR and IVDR
Live and Recorded | 60 Minutes
Introduction to Medical Devices and the New MDR and IVDR
- Definitions and actors
- Competent Authorities and Notified Bodies
- Economic operators – obligations of manufacturers, distributors, importers and authorised representatives
- Placing on the market and enforcement
- Introduction to the MDR & IVDR and reasons behind their development
- Chief differences of MDR with MDD and the impact of MDR on the industry
- What isn’t covered in the regulations?
- Eudamed database/GMDN
Register for the free Module 1 by completing the form below. You will be sent joining instructions and more information about the course (agenda, trainers, pricing etc).