In cooperation with our Swiss Partner – Luzern Baar Consulting, we’re delighted to invite you to attend our exclusive webinar session: New reality after MDR implementation – what can you expect? which will take place on June 17 at 11 AM CET.
Our expert Michał Timler will cover the following topics during the webinar:
– The difference in MDR before and after the changes. Do you have to change your QMS completely? What does it mean to introduce clinical trials? Are we going to have “pharma serialization” in MD?
– How can you adapt to the changes in MDR? – Preparation of Transition Plan, 12 major steps to be ready for new MDR regulations.
– How will the changes in regulations affect you? Which new processes, procedures and SOP are we going to follow? Do we have to change our production lines?
Click HERE to register!