Friday, 21 September 20186:00-8:00 pm CDTEmergo by UL Headquarters2500 Bee Cave RoadBuilding One, Conference Room B120Austin, TX 78746+1 512 327 9997
Come engage with professionals from your local regulatory community for an interactive presentation on how to prepare for the new EU MDR. The new regulation introduces more stringent clinical and post-market surveillance requirements for medical device manufacturers, regardless of risk classification. Come join us to learn strategies that can help your device company navigate the higher level of scrutiny, including:
This event is coordinated by the RAPS Texas chapter and is intended to encourage knowledge sharing and community development. A light meal will be provided and RAC holders may claim two RAC recertification credits.
Featured Speaker:Anna Calleja, MHS, cCE, cardiologist, clinical reviewer, TÜV SÜD
Registration Information:RAPS Members: $25Nonmembers: $40