Michigan Medical Device Summit - Session 2
Global Medical Device Regulation To Watch
The medical device industry has been challenged against the backdrop of a pandemic that continues to wreak havoc on global healthcare systems. Significantly, device manufacturers, whether big or small, face changes in how their products are regulated and certified. Hear the latest on regulatory trends across the foreign landscape and what they mean for product development, production and post-production activities, quality management systems, data collection, post-market surveillance, and more.
Kim Trautman - Medical Device, IVD and Combination Product Expert & Former Associate Director for International Affairs, Center for Devices & Radiologic Health, U.S. Food & Drug Administration
Advancing Healthcare and Improving Lives Through Medical Technology
The Michigan Medical Device Summit is a gathering of thought leaders, innovators, providers, and change-makers to discuss critical issues facing the state’s medical technology sector. The medical device industry was upended as the Covid pandemic raged, resulting in expansions, pivots, and recalibration – but business went on, it had to for most. The Summit will provide strategic insights on the latest in medical device innovation and manufacturing, regulation and compliance, supply chains, market access, and more. OEMs, contract suppliers and providers, academics and other professionals involved in Michigan’s medtech sector can garner new knowledge, tactics and best practices, while making valuable connections in this interactive event.