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
Metadata Management & Content Searchability in Life Sciences In the complex and data-rich environment of life sciences, effective metadata management is not just a nice-to-have—it's a necessity. Lisa Om - December 5, 2024 Blogs Biotech, CMO, CRO Clinical, Information Technology
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
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
Data Integrity in Life Sciences Discover best practices to improve and maintain data integrity in the AI era, focusing on compliance, patient safety, and effective data management. Lisa Om - November 24, 2024 Blogs Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Quality Assurance, Regulatory
