Course participant reviews for Introduction to Regulatory Affairs for Medical Devices
Average rating 5
Based on 5 reviews.
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Clinical Trial Manager, Europe, Moximed International GmbH
23 Jun 2020
Excellent overview
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...
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.
Consultant
23 Jun 2020
Comprehensive
Comprehensive course on New Regulation covering range of topics.
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
The course was very interactive with lots of opportunity to ask questions. It provided an excellent overview.