Thursday, 22 March 2018
5:30-8:30 pm EST
Stryker Orthopaedics – Homer Stryker Center Building
325 Corporate Drive
Mahwah, NJ 07430
The new European Medical Device Regulations (MDR) came into force May 2017, with full implementation deadlines set for May 2020. The MDR will replace the EU's current Medical Device Directive and understanding the new regulation is critical to manufacturers doing business in the European Union. This presentation will cover the major changes in the regulatory framework and ways in which device manufacturers are developing plans to meet these changes as well as determine the impact on their business.
The New York/New Jersey chapter invites you to join others from the local regulatory community to explore these changes, discuss what it means for manufacturers and regulatory professionals and explore ways to comply in this ever-changing environment. Light refreshments will be available to all attendees. RAC holders may claim two RAC recertification credits.
Robert Lally, senior director, regulatory affairs, Stryker Joint Replacement Division
RAPS Members: $25