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’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
Five Tips for Successful Veeva Implementation Blog article topic: Five Tips for Successful Veeva Implementation. Donald Zinn - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
