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Course participant reviews for Advanced Regulatory Affairs for Medical Devices

Average rating 4.6

Based on 5 reviews.
Reviews are published according to our review policy.
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Technical Manager, JensonR+ Limited
5/5
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.

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

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

Head of Project Management, Team Consulting
4/5
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.

QA Engineer, Welland Medical
5/5
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.

Quality & Regulatory Affairs Engineer, Welland Medical
5/5
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