USDM’s Guide to 21 CFR Part 11 Learn about 21 CFR Part 11, the FDA regulation ensuring the security, traceability, and compliance of electronic records and eSignatures in life sciences. David Blewitt - April 14, 2024 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
Elevating Life Sciences with the Cloud Assurance Certified Program Discover how USDM's Cloud Assurance Certified program ensures compliance, reduces risks, and drives innovation for life sciences organizations. Kim Hutchings - April 8, 2024 Blogs Biotech, Medical Device, Pharma Information Technology, Quality Assurance
Top 10 Considerations for Implementing a GxP Content Management System Discover the top 10 considerations for implementing a GxP-compliant content management system to enhance compliance, efficiency, and data management. Hovsep Kirikian - April 5, 2024 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
Veeva MedTech 2024 in Austin Join Veeva and USDM at Veeva MedTech Summit in Austin from April 29th to May 1st. Jay Crowley will be speaking on Holistic Data Management. Lisa Om - April 4, 2024 News & Events Medical Device Information Technology, Regulatory
ServiceNow Knowledge24 – Life Sciences Lunch & Learn Life Sciences Luncheon | Join ServiceNow & USDM Life Sciences at Knowledge24 Lisa Om - March 28, 2024 News & Events Biotech, Medical Device, Pharma Information Technology
USDM Life Sciences at Validation University By KENX, Validation University is a 3 day conference that shares knowledge & best practices for validation in life sciences. Ryan McDonald - March 18, 2024 News & Events Biotech, Medical Device, Pharma Information Technology
