Recorded June 7, 2017 | On-Demand Webinar
The new EU Medical Device and IVD Regulations, recently published in the Official Journal of the European Union on May 5, 2017, have set into force a series of compliance deadlines and processes that include three- and five-year transition periods. This webinar will cover the major points in the regulations, practical tips to help industry absorb the regulatory changes, as well as timing and other considerations for medical device and pharmaceutical manufacturers as products are transitioned into compliance before the new regulations come into force.
Sarah H. Stec, Associate, Squire Patton Boggs
Phil Johnson, Senior Director, Quality Compliance Services, QuintilesIMS