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New EU Medical Device Regulations - What's The Impact?

by Janice Kitchen (2020-04-19)


over china <strong>we<\/strong>re extremely excited and felt greatly proud of ourPartially as a result of the Poly Implant Prothese breast implant scandal, where a French manufacturer substituted approved medical-grade silicone with industrial-grade silicone that ruptured causing a variety of serious medical implants up to and including death, the European Commission began developing changes to their Medical Device Directives to prevent this type of an issue from happening again. The changes resulted in the drafting of a totally new Medical Device Regulation that was fully released this past February.

The new EMDR is the most extensive medical device regulation Europe has seen since the 1990's. Industry experts are concerned that regulations will increase costs and eliminate early access to device innovations that patients in Europe currently experience.

Understanding the contents of this regulation and its implications is crucial to the effective design, development, marketing, and utilization of medicals devices in the EU.


The current Medical Device Regulation stands at 350 pages and is a complex array of regulations written in the normal legalese. There are many changes that anyone designing, manufacturing, and/or marketing medicals devices into the EU needs to be aware of when compared to the original Medical Device Directives. This webinar will detail the changes and discuss their implications, and provide a greater understanding of the regulation medical device manufacturers.


At the completion of this webinar participant's will be able to:

Explain how the new Medical Device Regulation is structured

Define/explain the key sections of the regulation.

Explain the transition process from the Medical Device directives to the current Medical Device Regulation

Define the key differences between the MDD and the new MDR to include - notified bodies, clinical evidence, pre-market, transparency and traceability, governance and oversight

The and descript the changes to regulations from the Medical Device Directives.

Define the process and options for conducting the conformity assessment.

Explain the expanded role of the notified body.

Explain how this new regulation will impact US companies.


Pharma Times Magazine has called the new EU medical device regulation "A new landscape for medicaldevices." The new regulation has provided manufacturers and regulators alike with a much broader definition of both medical devices and in vitro diagnostic medical devices. This much broader definition will contribute to a significant improvement of medicals device products in terms of patient and user safety, device reliability, and overall quality


Anyone involved in the design, development, marketing, and management of medicals devices in the European Union. The specific positions and functions are varied and not restricted to any one function or job title.

Audit and Compliance Personnel / Risk Managers

Research and Development Engineers

Vice-Presidents, Directors, and Managers of medicals device design functions

Medicaldevice marketing personnel

For more detail please click on this below link:


Charles H. Paul is the President of C. H. If you have any concerns concerning where and ways to utilize At Richdales Institute we have been providing professional complementary medicine training to students from training venues in West London for 25 years., you could call us at the web site. Paul Consulting, Inc. - a regulatory, training, and technical documentation consulting firm. Charles has been a regulatory consultant to the life sciences industry for over 20 years and has published numerous white papers on the subject. The firm works with both domestic and international clients designing solutions for complex human performance problems.