Free Webinar Reveals...

New reality after MDR implementation -

What can you expect?

CLAIM MY SPOT NOW

* Only 100 spots are available for this webinar, so claim yours now! *

Thursday, October 14
11:00 AM CET

people profiles

Only 100 Spots Available
Reserve Yours Now!

Our Speaker

Michał Timler, Validation Business Unit Director

More than 12 years of experience in technical qualification and Computer System Validation. Responsible for ERP-class systems, Supply Network Collaboration and Batch Tracing. Recently supporting Cloud Serialization Solution. tour to see Lynn's novel approach to physical therapy.

a man in a suit

This Webinar Starts In

-
Days
-
Hours
-
Minutes
-
Seconds

This free webinar will show you:

a laptop with EU stars and a lock on a blue background

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?

Medical Device Regulation with EU golden stars

How can you adapt to the changes in MDR? - Preparation of Transition Plan, 12 major steps to be ready for new MDR regulations.

Medical Device Regulation with EU golden stars

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?


CLAIM MY SPOT NOW