IT & Regulatory Compliance for Life Science Manufacturers

Veeva R&D Quality Summit 2022 

As a Premiere Services Partner, USDM has been helping Veeva customers reduce their implementation and validation time since 2015, with over 200 Veeva projects successfully completed. Visit our booth at Veeva’s R&D and Quality Summit in Boston.

Darlene Limtiaco
- September 19, 2022

News & Events

Biotech, Clinical Research Organization, Contract Manufacturing Organization, Medical Device, Pharma

Clinical, Information Technology for Life Science Organizations, Manufacturing, Quality Assurance for Life Science Organizations, Regulatory

UDI Beyond Borders

UPCOMING VIRTUAL CONFERENCE: The 12th annual UDI Conference will be hosted virtually by USDM Life Sciences and moderated by Jay Crowley, the original developer and author of the FDA’s UDI requirements. Register for this complementary event on Nov 9, 2022.

Webinars

Medical Device

Manufacturing, Regulatory

Global UDI Data Management – The New Paradigm

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.

Webinars

Medical Device

Manufacturing

Veeva’s MedTech Summit 2022 | Minneapolis, MN

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.