EUDAMED Challenges for Medical Device Manufacturers: Future-Proof Your 2025 Compliance Strategy Discover how to streamline EUDAMED compliance and UDI registration. Learn from USDM & BYRD Health before the 2026 deadlines hit. Webinars Medical Device Regulatory
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 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
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
