The EU AI Act Is Here: What Life Sciences Companies Need to Know Now The EU AI Act is here. Learn what life sciences companies must do now to ensure compliance, avoid penalties, and stay ahead in a rapidly evolving regulatory landscape. John Petrakis - July 9, 2025 Blogs Biotech, Medical Device, Pharma Clinical, Information Technology
Security Over Speed: Applying J.P. Morgan’s Cyber Risk Mandate to Life Sciences Vendors Why life sciences must prioritize security over speed—and how smart TPRM strategies protect data, compliance, and patient safety. Brian Rankin - May 2, 2025 Blogs Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology
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
