Jay Crowley, Architect of FDA’s UDI Rule, to Answer Medical Device Manufacturer’s Questions at UDI Conference

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Crowley had primary responsibility for the development and implementation of the FDA’s UDI system.

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Device manufacturers are still working on UDI implementation, but the process brings up questions about compliance, the Global UDI Database and labeling and other device specific challenges.

USDM Life Sciences, the leading global professional services firm for Life Science and Healthcare organizations, is pleased to announce Jay Crowley will answer questions from medical device manufacturers about UDI compliance at this year’s UDI Conference.

“Device manufacturers are still working on UDI implementation, but the process brings up questions about compliance, the Global UDI Database and labeling and other device specific challenges,” said Crowley. “I’m looking forward to discussing the challenges and concerns of the medical device manufacturing community at the conference.

As Vice President of UDI Services and Solutions at USDM Life Sciences, Crowley and the team of USDM Life Sciences Professionals, help 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.

Meet with Jay Crowley and the USDM Life Sciences UDI Team

  •     When: April 18-19, 2016
  •     Where: Hilton Baltimore in Baltimore, MD
  •     Booth: #8

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 http://www.usdm.com.

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Ryan Carmel
USDM Life Sciences
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