Fast-Track Your Journey to Commercialization Fast-track commercialization in life sciences with USDM's GxP expertise, IT strategies, and QMS frameworks for compliance, efficiency, and success. Lisa Om - March 25, 2024 Blogs Biotech Clinical
USDM Sponsors Veeva R&D and Quality Summit 2023 Ryan McDonald - July 31, 2023 News & Events Information Technology, Quality Assurance
GxP System Validation and Monitoring for Half the Cost Learn how an emerging therapeutics company saves more than $400k annually and maintains SaaS systems for half that cost. Lisa Om - June 6, 2023 Case Studies Biotech Information Technology
Veeva & USDM at Veeva MedTech 2023 in Chicago Join Veeva and USDM at Veeva MedTech Summit in Chicago at May 30 to June 1st. USDM will be speaking. Join us there! Ryan McDonald - March 10, 2023 News & Events Medical Device Information Technology, Regulatory
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. Lisa Om - May 17, 2022 News & Events Medical Device Information Technology, Manufacturing, Regulatory
Veeva Vault Implementation to Maximize GxP Uses Case study on Veeva Vault Implementation to Maximize GxP Uses. Hovsep Kirikian - April 18, 2022 Case Studies Biotech Clinical
