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Course participant reviews for Advanced Regulatory Affairs for Medical Devices

Average rating 4.6

Based on 5 reviews.
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5/5
Technical Manager, JensonR+ Limited
16 Feb 2017
Interactive course

I felt the course was very interactive, intimate (not too many delegates) and it was the correct duration for the course.

4/5
Senior Regulatory Affairs Specialist (EMEA & Canada), HOLOGIC LTD
16 Feb 2017
Detailed course

The detailed content was broken down into bitesize chunks. The course was engaging and covered a variety of topics.

4/5
Head of Project Management, Team Consulting
16 Feb 2017
Great course

There was a small class and it had really good detailed sessions. I took this course to gain an understanding of the old vs new MDR.

5/5
QA Engineer, Welland Medical
16 Feb 2017
Excellent course

There was good structure with specific references to documents to follow up with details. All the information related to the new MDR which was great.

5/5
Quality & Regulatory Affairs Engineer, Welland Medical
16 Feb 2017
Workshops were great

I enjoyed the workshops the most. I found them to be a very useful tool to test the knowledge we learned. I took this course as it was directly related to my job role.

Displaying 1-5 of 5 reviews