Seamless Compliance and Cost Savings with USDM’s Veeva-DocuSign Integration Accelerator Learn how USDM’s Veeva-DocuSign Integration Accelerator simplifies eSignatures, reduces costs, and ensures 21 CFR Part 11 compliance for life sciences. Darlene Limtiaco - February 21, 2025 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Quality Assurance
Streamlining Clinical Trials with the LLM Protocol Assistant LLM Protocol Assistant improved clinical trial efficiency, reducing costs by $250K annually, cutting protocol queries by 70%, and accelerating timelines by 15%. Darlene Limtiaco - December 2, 2024 Case Studies Biotech, Pharma Clinical, Information Technology, Regulatory
Best Practices for Managing Content in Emerging Biopharma and Regulated Life Sciences Companies Streamline content management for emerging biopharma with best practices to ensure compliance, scalability, and operational excellence Lisa Om - November 25, 2024 Blogs Biotech, Pharma Clinical, Information Technology, Research & Development
Leveraging AI for Enhanced Clinical Trial Data Management in Life Sciences Discover how AI enhances clinical trial data accuracy, saves $200K annually, reduces manual effort by 80%, and accelerates timelines by 25%. Mark Gancsos - July 25, 2024 Case Studies Biotech, CRO, Pharma Clinical
USDM Sponsors Veeva R&D and Quality Summit 2024 Connect with USDM at the Veeva R&D and Quality Summit in Boston. We've got innovative ideas to share with you! Michelle Gardner - July 23, 2024 News & Events Information Technology, Quality Assurance
USDM Life Sciences at Veeva R&D and Quality Summit – Madrid Veeva R&D and Quality Summit - Madrid Join us at the Veeva R&D and Quality Summit and explore ways to gain the most value from your Veeva investment. Ryan McDonald - April 29, 2024 News & Events
