Medical Device made Easy Podcast

You may be on the business of Software development and you ask yourself why your Dev team is not really happy to work with Quality and Regulatory affairs team? In this episode, we will discuss with Ch...

20 Kesä 20230s

Since the EU MDR extension was voted, there are still a lot of questions remaining. This is what we will try to clarify today with Florian Tolkmitt from Pro-Liance. This podcast will provide you some ...

13 Kesä 20230s

Medical Device News - june 2023 regulatory update The post Medical Device News -June 2023 regulatory update appeared first on Medical Device made Easy Podcast. hamza benafqir

8 Kesä 20230s

We all need to keep ourselves up to date. But how to access reliable information and how often should a check be done. This is what we will discuss with Ivan Perez Chamorro from MedBoard. You will get...

30 Touko 20230s

I know this is not really something that people anticipate. But the EU MDR is asking you to anticipate that. So don’t miss this as this can raise a Non-Conformance from the Notified Body during an aud...

23 Touko 20230s

Technical Files inconsistency, it is when your technical file is not providing the right information or that all the information is not aligned. Here we will try to look at some of these issues. The p...

16 Touko 20230s

We hear so many things about UK and the timeline and now that EU issued an extension, the question is “Does this change something for UK” So on this episode we’ll review again what are the requirement...

9 Touko 20230s

Medical Device news - May 2023 Regulatory Update- easy medical device The post Medical Device news – May 2023 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir

5 Touko 20230s