Jay Crowley Leads UDI Implementation Workshop at UDI Conference

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Crowley is Architect of FDA’s UDI Rule and VP of UDI Services and Solutions at USDM Life Sciences

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I also want to make sure organizations are taking advantage of all the benefits of the UDI system and get all their questions answered.

USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is pleased to announce Jay Crowley will lead their Hands-On UDI Implementation Workshop immediately following the UDI Conference. The workshop will be an opportunity for medical device manufacturers to understand how to apply the Unique Device Identification (UDI) Rule to their product portfolio and get answers to their questions. Participants are encouraged to bring examples of labels and packages for review.

“I look forward to continuing to work with the medical device community to ensure UDI compliance by the UDI Rule deadline,” said Crowley. “I also want to make sure organizations are taking advantage of all the benefits of the UDI system and get all their questions answered.”

As Vice President of UDI Services and Solutions at USDM Life Sciences, Crowley helps medical device manufacturers achieve regulatory compliance as well as internal benefits and competitive advantage with UDI implementation.

Crowley held various positions over nearly 27 years at the FDA. Most recently, he was Senior Advisor for Patient Safety, in the FDA’s Center for Devices and Radiological Health. Crowley had primary responsibility for the development and implementation of the FDA’s UDI system.

USDM Life Sciences Hands-On UDI Implementation Workshop:

  • When: Wednesday, April 20, 2016, 8:30am – 5:00pm
  • Where: Hilton Baltimore in Baltimore, MD
  • Cost: $1950/person, $500 for others joining from same company
  • Day after UDI Conference at same location
  • For more information, visit our website

About USDM Life Sciences:
USDM Life Sciences has more than 16 years of experience supplying clients in the life science and healthcare industries with compliance services while partnering with best of breed organizations to help companies simplify, unify and optimize their business and compliance objectives. USDM Life Sciences is a leading global regulatory consulting firm providing compliance, validation, qualification, quality, auditing and information technology services via project teams and staff augmentation to our clients in the medical device, biotechnology, biologics, diagnostics and pharmaceutical industries. For more information, please visit usdm.com.

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Ryan Carmel
USDM Life Sciences
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