ON-DEMAND WEBINAR: We share compliant IT strategies for early-stage biotech and pharmaceutical organizations, helping you to rethink your challenges and develop an IT strategy from the pre-clinical phases through commercialization.
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 waw hosted virtually by USDM Life Sciences and moderated by Jay Crowley, the original developer and author of the FDA’s UDI requirements. Watch now.
ON-DEMAND WEBINAR: Currently, multiple regulators have or are launching national UDI Databases (US, EU, SFDA, NMPA, KFDA, HSA). Other regulators are following close behind. The new UDI challenge for device manufacturers is creating and submitting the required data to these national databases and maintaining this data – and regulatory compliance – over time.
