Medical Alley Association and its partners Investissement Quebec and the Quebec Government Office in Chicago present a seminar on global regulation and U.S. reimbursement. Register for three sessions covering U.S. Regulatory, EU/Asia Regulatory, and U.S. Reimbursement for a primer on key topics in today's environment
Part 1: U.S. Regulation of Medical Products
Medical Devices and Digital Health products face a range of regulations in the United States, primarily from the Food & Drug Administration (FDA). In this session, you will learn the latest on FDA regulations and strategies to employ in launching your first product in the U.S.
Cori Ragan, M.S, Regulatory & Quality Systems Principal Advisor
Part 2: EU Regulation of Medical Products
Medical Devices and Digital Health products face a range of regulations across the European Union. In this session, you will hear the latest on the EU’s Medical Device Regulation and strategies to launch your products.
Speaker: LOK North American
Louis-Paul Marin, President and Founder
Part 3: U.S. Reimbursement Seminar
Reimbursement, or payment for various health services, in the U.S. differs significantly compared to most other countries. A mix of public and private, national and regional, and separate medical, dental, vision, and pharmacy benefits means your path to securing payment can be complex and fraught with risk. In this session you will learn the fundamentals of U.S. reimbursement and how to pursue it for your company.
Tom Hughes, Health Economics and Reimbursement Senior Principal Advisor