Jay spent 26 years at the FDA, and he developed the requirements for the FDA's UDI system and was one of the authors of the US UDI rule. Jay explains what the delay of enforcement for some class I devices in the US means. Jay Crowley, VP and UDI Practice Lead at USDM Life Science What we talked about: What are the details of the new UDI and MDR requirements  Determining your organization's requirements Strategies to implement adapted practices Find this interview and many more by subscribing to Life Sciences Accelerated, on Apple Podcasts, on Spotify, or on our website.