Course participant reviews for Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations
Average rating 4.5
Very good webinar in term of content, presentation and speakers. Lots of extra material made available by the presenters
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.
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...
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...
Good course
The course covered a vast area, and it was helpful to follow new requirements/changes.
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...
The seminar was very good, the speakers and slides were very professionals and it covers wide aspects of the learned subjects.
I enjoyed the webinar very much, both presenters were very good and showed their depth of knowledge.
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...
Both speakers were really good and brought the needed perspective to the discussion.
Good
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...
The course is well thought and based on the expert's experiences.
Good course, very interesting and complete overview with speakers that bring the insights of both an ex-auditor and an industry representative.
A good intensive course - I would recommend for my colleagues especially who need a general understanding of MDR impact on medical SW.
A very interesting and informative course. Excellent speakers
One of the best training courses I have attended.
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!
Engaging delivery of the subject by speakers who clearly had extensive knowledge and experience of medical device software in a regulatory environment.
Big thank you to Koen! He shared the latest information of the risk classification guidance.
Koen brought a lot of practical industry experience which was extremely useful.
A well structured, well presented programme
Good course. A lot of information in detail.
Overall I am satisfied. Well organized and good quality of speakers and materials