
What does a strategy for regulatory compliance looks like?
In this episode, Adam Isaacs Rae will help us shape your Regulatory Compliance Strategy. This is a requirement of the EU MDR and IVDR but it doesn’t provide much information. So let’s review that toge...
24 Okt 20240s

What are the TOP 3 issues on CAPAs?
In this episode, Georg Digel will help use solve 3 major problems with our CAPAs. He will tell you what these problems within your Quality Management System are and propose some solution. We will also...
17 Okt 20240s

Medical Device News, October 2024 Regulatory Update
Medboard: https://www.medboard.com/ EUROPE EVENTS NB ROW Middle East Northern America South America: PODCAST Social Media to follow The post Medical Device News, October 2024 Regulatory Update appeare...
10 Okt 20240s

How to select the best plastic for your Medical Device?
In this episode, Lucas Pianegonda will help us to select the right material for your medical device and answer questions that you maybe would love to hear his answer. We will also talk about sustainab...
3 Okt 20240s

UK vs EU vs US – How to switch to another region easily?
In this episode, Claire Dyson will give us the recipe to launch correctly your Medical Device when you go abroad and for that we will take the example of EU and US. The post UK vs EU vs US – How to s...
24 Sep 20240s

How to do a PMCF Literature Search for Medical Devices?
In this episode, Cesare Magri will try to improve our skills on PMCF literature search. We will investigate on the misconceptions and what people should make to do it right. The post How to do a PMCF...
17 Sep 20240s

Medical Device News, Septembre 2024 Regulatory Update
EU Switzerland Training Events: ROW Medical Device Live Expert: Podcast The post Medical Device News, Septembre 2024 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqi...
10 Sep 20240s

How to use AI GPT for your Quality and Regulatory work?
n this episode, Martin King will share with us his practice of AI in the context of Quality and Regulatory affairs for medical devices. This will explain to you some best practices to maintain to avoi...
5 Sep 20240s



















