Date(s) - 09/21/2019 - 09/24/2019
Pennsylvania Convention Center
NAMSA invites you to join us at the RAPS Regulatory Convergence Conference on September 21-24, 2019 in Philadelphia, PA. This annual regulatory event is one of the largest for medical device professionals and includes knowledge sharing, education and training from some of the best minds in industry.
Complimentary Consultations (Booth #403)
Throughout this event, NAMSA will have a regulatory expert available for 30-minute complimentary consultations. We welcome the opportunity to discuss with you the most cost-effective regulatory pathway to market based on your unique product development requirements. We’ll also walk you through our latest case study with French biosurgical firm, Biom’Up, and help you understand how NAMSA provided the organization savings of $17M and 23 months in PMA development timelines (read case study here).
Please email us at email@example.com to reserve your consultation time, or simply stop by Booth #403 in the exhibitor area to meet with us.
Scientific Session: Managing the Requirements of the EU Medical Device Regulation General Safety and Performance Requirement 10.4.1
Date/Time: Monday, September 23, 2019 | 2:05 PM – 3:00 PM ET
Lead by: Adrian Keene, Director of Development Strategy and Manager of Regulatory/Quality-EMEA