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Jay Crowley is currently Vice President, UDI Solutions and Services, at USDM Life Sciences. He developed the framework and authored key requirements for the U.S. Food and Drug Administration’s (FDA’s) Unique Device Identification (UDI) System and is a globally recognized UDI subject matter expert.
View Jay Crowley’s profile on LinkedIn, a professional community of 1 billion members. USDM is changing how compliance is addressed for life science companies worldwide. We are…
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Feb 19, 2014 · CDRH patient safety senior advisor Jay Crowley has retired from FDA to join regulatory consulting firm USDM Life Sciences as vice president of its unique device identification (UDI) practice. At FDA, Crowley developed the framework and authored key requirements for the agency’s UDI system.
May 13, 2014 · USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Jay Crowley, Vice President of the Unique Device Identification Practice,...
Apr 16, 2018 · FDB recently interviewed Jay Crowley to get his expert perspective on the Unique Device Identification (UDI) system. Crowley developed the framework and authored key requirements for the Food and Drug Administration’s UDI system while working as the Senior Advisor for Patient Safety in the FDA’s Center for Devices and Radiological Health.
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Dr. Jay Croley, MD is an orthopedic surgeon in Houston, TX and has over 10 years of experience in the medical field. He graduated from University of Texas Medical Branch in 2013. He is affiliated with Houston Methodist Clear Lake Hospital. He is accepting new patients and telehealth appointments.
