Listen "The MDR No Good Very Bad Day: Go To Market Challenges in the EU"
Episode Synopsis
It used to be that Europe was the first choice when bringing a product to market. Relaxed regulation meant a quick approval and the chance to earn some money while waiting for FDA approval. That's not the case anymore, and thanks to MDR, there are new challenges and roadblocks - not to mention a LOT more expense - involved in bringing a medical device to market in Europe.
More episodes of the podcast RAQA Today
Inside the FDA: Pre-Subs, Wellness Devices & Cybersecurity Challenges | leanRAQA Today | S5:E5
25/09/2025
Rise of the Regulatory Rebel
23/09/2025
EU MDR - More then Just Red Tape?
03/09/2025
Wait, What - There are Rules?!?!?
26/08/2025
ZARZA We are Zarza, the prestigious firm behind major projects in information technology.