Medical Device Product Life Cycle – 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!!
𝗕𝗲𝗶𝗻𝗴 𝘁𝗵𝗲 ‘𝗣𝗲𝗿𝘀𝗼𝗻 𝗥𝗲𝘀𝗽𝗼𝗻𝘀𝗶𝗯𝗹𝗲 𝗳𝗼𝗿 𝗥𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗖𝗼𝗺𝗽𝗹𝗶𝗮𝗻𝗰𝗲’ – 𝗶𝘀 𝘁𝗵𝗶𝘀 𝗶𝗻 𝗳𝗮𝗰𝘁 𝗮 𝗾𝘂𝗮𝗹𝗶𝘁𝘆 𝗰𝗼𝗻𝘁𝗿𝗼𝗹, 𝗿𝗲𝗴𝘂𝗹𝗮𝘁𝗼𝗿𝘆 𝗮𝗳𝗳𝗮𝗶𝗿𝘀, 𝗼𝗿 𝗯𝗼𝘁𝗵?
How can and should the requirements on the PRRC ‘Person Responsible for Regulatory Compliance’ be managed? The MDCG Guideline doesn’t 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 👇🏻
We are looking forward to meeting you at Medicon Village in Lund!