Theresa Jeary

Was very useful. I feel I accomplished further knowledge about the implementation of MDR and IVDR and also what is on the horizon in terms of the UK regulations from the course. The content of update on IVDR was great as it was directly related to my work. I also enjoyed learning more about the history of the regulations/legislative process and gained some useful background knowledge on combination products.

Very good course.

The webinar was presented very well with both speakers having a clear understanding of the changes and implications that the MDR will have. Both speakers were able to help with all questions with a clear understanding of their answers and applicability. Both speakers were very clear and very helpful with all questions and all parts were very informative, i really liked the workshops.

It was really good: content was clear, presentation was good, and speakers were interesting

Speakers are very knowledgeable about Medical Device products. Janette also gave us extra material that will help me navigate European regulations and explore new content.

Very good

It was really good: content was clear, presentation was good, and speakers were interesting

It was well structured, informative and interactive. well structured and concise presentation, information easy to follow. the speakers - well prepared and friendly

Excellent course material/ presentations, clear, easy to understand and straight forward. Very welcoming and friendly speakers, with an open minded mentality to consider different regions in covering medical devices regulations. Would highly recommend the course for basic/intermediate level manufacturers and regulators.

All 3 speakers were fantastic and I really liked that they were all coming from different sides of the industry, sharing their perspective on top of delivering the content