Taking the Pulse of UDI Compliance: Final Survey Results

So how are medical device professionals managing UDI compliance? What challenges do they still face?

With another deadline fast approaching, now’s a good time to see how you compare with your peers in meeting regulatory and labeling requirements.

Download this webinar featuring, Jay Crowley from USDM Life Sciences, as we review results from a recent survey of the Medical Device Industry. As a noted authority on UDI, Jay will provide valuable insight drawing from his experience at the FDA working with companies on their UDI programs. See what it takes to achieve sustained compliance with a validated Enterprise Labeling Solution.

• See where companies are with UDI compliance and the Sept. 24^th deadline
• Hear about ongoing technology and regulatory challenges
• Compare your labeling approach with those cited by your peers
• Gain real-world insight into best practices for achieving sustained compliance
• Learn how to reduce the time and cost of implementing a validated labeling solution

speakers

Jay Crowley, Vice President of UDI Services and Solutions, USDM Life Sciences
Jay Crowley is the Vice President of UDI Services and Solutions at USDM Life Sciences. Jay was Senior Advisor for Patient Safety in the Food and Drug Administration’s Center for Devices and Radiological Health. Jay developed the framework and authored key requirements for the FDA’s Unique Device Identification system.

Craig Hodgson, Industry Manager, Loftware
Craig manages all industry-specific engagements, relationships, and partnerships at Loftware. His knowledge of the Enterprise Labeling Industry is vast and spans a wide range of industries including Medical Device, Pharmaceuticals, and more.