février 02, 2022 - février 03, 2022
Date: 2 and 3 February, 2022
Time: 09.50 - 15.20 CET
Consultant: Mindy McCann
Join Mindy McCann on February 2nd for the session 'Major Regulatory Compliance Challenges for the non-European Industry', starting from 12:40 - 13:10. The new European regulations have presented the medical device industry with new challenges in order to ensure compliance to the MDR/IVDR and continue placing medical devices on the EU market. This session will identify some unique key challenges experienced by non-European medical device manufacturers in preparing for compliance to the MDR/IVDR, and the lessons learned and/or strategies being used by medical device manufacturers to address these challenges.
For more information about the Conference and to Register, please visit the EAAR Conference website.