ON-DEMAND WEBINAR: Please watch our panel of experts, including Francisco Vicenty, Program Manager, Case for Quality, FDA, discuss any changes and implications impacting medical devices, pharma, and biotech organizations.
ON-DEMAND VIRTUAL CONFERENCE: The 12th annual UDI Conference was hosted virtually by USDM Life Sciences and moderated by Jay Crowley, the original developer and author of the FDA’s UDI requirements. Watch now.
Phased migration of critical applications and databases addresses the move of highly complex, external facing GxP applications while controlling access to sensitive data.
Join USDM's Jay Crowley to discuss the growing UDI landscape, the similarities and differences of various UDI regulations, and their impact on MedTech organizations.
