Medical Device Product Life Cycle โ a conference for QA & RA professionals!
Let’s welcome our next speaker in line , Ase Ek, Senior Consultant and Trainer at Key2Compliance to our Medical Device Product Life Cycle conference!!
๐๐ฒ๐ถ๐ป๐ด ๐๐ต๐ฒ โ๐ฃ๐ฒ๐ฟ๐๐ผ๐ป ๐ฅ๐ฒ๐๐ฝ๐ผ๐ป๐๐ถ๐ฏ๐น๐ฒ ๐ณ๐ผ๐ฟ ๐ฅ๐ฒ๐ด๐๐น๐ฎ๐๐ผ๐ฟ๐ ๐๐ผ๐บ๐ฝ๐น๐ถ๐ฎ๐ป๐ฐ๐ฒโ โ ๐ถ๐ ๐๐ต๐ถ๐ ๐ถ๐ป ๐ณ๐ฎ๐ฐ๐ ๐ฎ ๐พ๐๐ฎ๐น๐ถ๐๐ ๐ฐ๐ผ๐ป๐๐ฟ๐ผ๐น, ๐ฟ๐ฒ๐ด๐๐น๐ฎ๐๐ผ๐ฟ๐ ๐ฎ๐ณ๐ณ๐ฎ๐ถ๐ฟ๐, ๐ผ๐ฟ ๐ฏ๐ผ๐๐ต?
How can and should the requirements on the PRRC โPerson Responsible for Regulatory Complianceโ be managed? The MDCG Guideline doesnโt provide much of an answer except that it is the responsibility of the manufacturer to ensure conformity of devices being released. We will take a deeper look into what it means, and methods that can be applied to demonstrate compliance, over time.
Find out more about our 2-day international conference, the speakers and how to get your ticket ๐๐ป
We are looking forward to meeting you at Medicon Village in Lund!