This webinar was presented live on Wednesday, March 21, 2018. Click below to watch on demand.
The E.U.’s medical device regulatory system is undergoing a major overhaul. This webinar will provide an overview of common European Union market entry requirements under the current MDD and the new MDR. Additional MDR requirements regarding clinical evaluations will be reviewed for their impact on placing products on the market. Strategies for ensuring market access will be discussed.
Featured Speakers:
Michael Lynch
Managing Consultant
Intertek USA
Danielle Kirsh
Assistant Editor
Medical Design and Outsourcing
Sponsored by:
