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Course participant reviews for Introduction to Regulatory Affairs for Medical Devices

Average rating 5

Based on 5 reviews.
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5/5
Clinical Trial Manager, Europe, Moximed International GmbH
23 Jun 2020
Excellent overview

The course was very interactive with lots of opportunity to ask questions. It provided an excellent overview.

5/5
Scientific Affairs European Manager, Moximed International GmbH
23 Jun 2020
Enjoyed the course

I was looking for a course which would inform and prepare me for the new MDR. The fact that we could ask questions that arose at any time was great; I enjoyed this course immens...

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5/5
Regulatory Affairs Officer, Barco N.V
23 Jun 2020
Good informal contact with trainer

The fact that it was a small group gave us the opportunity to discuss everything with good informal contact with the trainer.

5/5
Consultant
23 Jun 2020
Comprehensive

Comprehensive course on New Regulation covering range of topics.

5/5
Anonymous
07 Jun 2016

“There was clear information about classification, requirements and exercises.” Regulatory Affairs Team leader, Teva Pharma Nederland

Displaying 1-5 of 5 reviews