VIDEO: Shifting Global Regulations Hit Medical Device Manufacturers


Posted May 23, 2017

Federal regulators in the United States and the European Union are gearing up for a big shift in the way they approve and monitor medical devices. In this video, see how representatives from both sides of the Atlantic came together to discuss the potential ramifications of these changes.

Read more about the Symposium on the Evolving Standards and Regulatory Structure for Medical Devices, which was hosted on April 4–5 by AAMI, the Food and Drug Administration, and BSI.