ISO 13485:2016 & The Medical Device Regulation ( CE Marking Process) Reviews

Kevina was very knowledge on topics and extremely thorough. Didnt feel like content was overwhelming, for such huge topics. Very informative and thorough.

Excellent delivery, content very relevant and broken down

Great 2 days had for the course. Information was delivered clearly and was easy to follow

Kevina is very knowledgeable and engaging. She uses very relevant examples to explain the topics and ensures we have understood the topics.

Kevin brought a wealth of industry experience to bring context to the regulations and standards. Feel more confident in navigating through the MDR

thank you very much for a brilliant course. it was very informative and although it was a lot of information to take on however Kevina was extremely knowledgeable and very good at teaching us the most important parts to follow of the large regulations, and it was very good that Kevina could adapt the course as we went along to tailor it to our role in medical devices as a company.

Comprehensive seminar - with much content. Excercise in groups was really good

Very informative and relatable. Difficult subject to learn and train on but Kevina made it interesting and relevant to Aspens requirements.

This information provided was excellent

Good and informative.