Course participant reviews for Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations

Average rating 4.5

Based on 29 reviews.
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4/5
Conxi V
17 Oct 2022

Overall I am satisfied. Well organized and good quality of speakers and materials

5/5
Didier G
17 Oct 2022

Very good webinar in term of content, presentation and speakers. Lots of extra material made available by the presenters

5/5
Janine B
17 Oct 2022

This course contained excellent content and speakers. I enjoyed that it was interactive with case studies and quiz exercises to keep engagement up and check understanding.

5/5
Samuel P
17 Oct 2022

Fantastic course. Speakers were quite knowledgeable and were able to transmit the information in a great way. They were willing to answer all of our questions/doubts at any time...

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4/5
Louise R
25 Apr 2022

I wanted to learn the nuance of software as a medical device to support my role as a quality engineer for IVD's. I do feel more equipped now to provide recommendations to collea...

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4/5
Evie E
26 Oct 2021

Good course

4/5
Jitendra G
26 Oct 2021

The course covered a vast area, and it was helpful to follow new requirements/changes.

5/5
Luis M
17 Nov 2020

I think it has been very useful and interesting, and I believe most people has been involved and participating, which makes it lively and helps you keep in the flow when doing o...

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5/5
Avital L
17 Nov 2020

The seminar was very good, the speakers and slides were very professionals and it covers wide aspects of the learned subjects.

4/5
Sabrina S
17 Nov 2020

I enjoyed the webinar very much, both presenters were very good and showed their depth of knowledge.

5/5
Jennie M
20 Nov 2019

Both very good and enthusiastic speakers. It is very nice that they work with MDSW and have a lot of examples, which makes it more understandable. I liked the course and learne...

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4/5
Sandra B
29 Apr 2019

Both speakers were really good and brought the needed perspective to the discussion.

4/5
Arun M
29 Apr 2019
5/5
Suzanne M
29 Apr 2019

A very worthwhile introduction to the regulatory requirements of medical device software for anyone new to this device type. The course covered a broad range of relevant subject...

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4/5
Ana B
29 Apr 2019

The course is well thought and based on the expert's experiences.

5/5
Antoine N
29 Apr 2019

Good course, very interesting and complete overview with speakers that bring the insights of both an ex-auditor and an industry representative.

4/5
Camilla Inesa C
29 Apr 2019

A good intensive course - I would recommend for my colleagues especially who need a general understanding of MDR impact on medical SW.

5/5
Laura S
20 Nov 2018

A very interesting and informative course. Excellent speakers

5/5
Ben S
20 Nov 2018

One of the best training courses I have attended.

5/5
Cadence T
20 Nov 2018

This is one of the best training organised by Management Forum in term of the quality of the content and presenters. I am equipped to do my job!

5/5
Stephen M
20 Nov 2018

Engaging delivery of the subject by speakers who clearly had extensive knowledge and experience of medical device software in a regulatory environment.

4/5
Marika M
20 Nov 2018

Big thank you to Koen! He shared the latest information of the risk classification guidance.

4/5
Leon D
23 May 2018

Koen brought a lot of practical industry experience which was extremely useful.

5/5
Peter O
28 Nov 2017

A well structured, well presented programme

4/5
Jose F
28 Nov 2017

Good course. A lot of information in detail.

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