Jay Crowley

Jay Crowley (based in the US) is currently Vice President, Medical Device Solutions and Services – and UDI Practice Lead, at USDM Life Sciences. Prior to joining the firm in January 2014, Crowley was Senior Advisor for Patient Safety, in FDA’s Center for Devices and Radiological Health.  He held a variety of positions over his nearly 27 years at FDA.  Jay had primary responsibility for the development and implementation of US FDA’s Unique Device Identification System Regulation and the accompanying database (GUDID), as well as the development of the GHTF and IMDRF UDI guidance documents.  Jay supports a wide variety of stakeholders in the development and implementation of UDI and UDI data, including manufacturers, providers, and governments.