Join us for this advanced workshop at Cintas Center, Xavier University, Thursday, November 21, 2019, 8:30am-5:00pm EST to Friday, November 22, 2019, 8:30am-4:00pm EST
Experts Bassil Akra (TÜV SÜD), Gert Bos (Qserve), Kim Trautman (NSF), Stephanie Lauman (bioMérieux), and Lindsay Taylor (Abbott) will lead you through the development of a time-critical action plan for keeping your medical devices on the EU market using proven strategies and tactics. At this workshop, you will develop:
Advanced strategies to effectively work with notified bodies.
Insightful game plans for compiling the data required to certify your products.
Recommendation plans to heighten awareness of the urgency to take action and gain support from senior leaders (CEO, COO, CQO, CFO, Chief Legal Officer, etc.).
Walk away with practical solutions to successfully prepare your company for the fast-approaching regulation deadline of May 26, 2020.