An Introduction to the Medical Device Regulation
This seminar provides an invaluable overview of the European Medical Device Regulation (MDR). The interactive programme will explain the new legislation and which products are covered, the involvement of Notified Bodies and how to choose one and will outline a manufacturer’s responsibilities. It will also cover the documentation necessary to apply for the CE mark.
This is an excellent introduction from leading experts in the field and delegates should expect three days of intensive training.
For a more advanced follow-on course from this, please see our Advanced Regulatory Affairs for Medical Devices which you may also be interested in.
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Suitability - Who should attend?
Benefits of attending
- Learn an overview of EU regulations and the MDR
- Understand the classification and labelling system of medical devices
- Explore medical device vigilance
- Gain information on CE Marking
- Clarify drug/device combinations and devices incorporating material of animal origin
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Reviews by course attendees
Average rating 4.6
It was really good: content was clear, presentation was good, and speakers were interesting
Speakers are very knowledgeable about Medical Device products. Janette also gave us extra material that will help me navigate European regulations and explore new content.
About IPI Academy
International Professional & Industry Academy (IPI) is an international leading professional training organisation based in London. Our training solutions provide a return on your investment with measurable results, and are delivered by experienced professionals and managed with exceptional care and...
The webinar was presented very well with both speakers having a clear understanding of the changes and implications that the MDR will have. Both speakers were able to help with ...