Navigating ICH E6(R3) with Confidence – A New Standard for IT Governance in Clinical Research Watch on demand to discover how USDM’s CRO Assurance simplifies compliance with the new ICH E6(R3) sponsor oversight requirements. On Demand, Webinars CRO Clinical, Information Technology, Quality Assurance, Regulatory
USDM Life Sciences at the American Biomanufacturing Summit 2025 Join us in San Francisco to discuss AI-driven transformation for biomanufacturing excellence. Marium Amin - March 17, 2025 News & Events Medical Device Manufacturing
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
USDM Life Sciences Summit 2025 Watch on demand to discover AI, automation, and data strategies to drive innovation & compliance in life sciences. News & Events, Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Version Control & Audit Trails in Life Sciences Version control and audit trails are two fundamental mechanisms for maintaining data integrity and accuracy. Learn best practices. Lisa Om - December 5, 2024 Blogs Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Quality Assurance, Regulatory
Ensuring Continuous Compliance and Efficiency with Microsoft Azure DevOps Azure DevOps solution enabled a medical imaging company to achieve 100% compliance, save $150K annually, and streamline operations by 25%. Darlene Limtiaco - December 2, 2024 Case Studies Medical Device Information Technology, Manufacturing, Quality Assurance, Regulatory
