Are you attending?
We encourage you to join Jay Crowley’s UDI presentation. Before USDM, Jay held various positions at the FDA during his 26-year tenure and developed the framework and authored essential requirements for the FDA’s Unique Device Identification (UDI) System.
Jay will share insight into the growing UDI landscape, the similarities and differences of various UDI regulations, and their impact on MedTech organizations.
Veeva’s MedTech Summit
Minneapolis
Wednesday, June 1
11:00 am CT
Session: USDM: Managing UDI Compliance and Solving for Emerging Regulations
As a Premier Veeva Services Partner, USDM has a fully-aligned partnership with Veeva to address compliance and change management in the pharma and med-tech industries. Learn more here.
