))
020: Steve Vinson | Leading Change in Medical Devices
Manage episode 310398982 series 3054010
Content provided by Steven A. Vinson and PMP. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by Steven A. Vinson and PMP or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://player.fm/legal.
EU MDR and FDA's Case for Quality are just two of the initiatives impacting medical devices in 2019. According to the new EU MDR (European Union Medical Device Regulation), combination products must meet medical device standards. This is new. Listen to Steve's advice on where to get more information.
Also: How do you go from managing projects in dirty chemical plants to Healthcare IT projects to Medical Devices and back to Pharma? What is the difference between medical devices and pharmaceuticals? What are FDA and European Union medical device regulators doing in 2019 that Medical Device and Pharma professionals need to know about?
Mentioned in this episode:
email Steve for more info at steven.vinson@bpm-associates.com
36 episodes
Share
