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
EUDAMED Compliance: Your Most Pressing Questions—Answered Get expert answers to top EUDAMED compliance questions and learn how to avoid costly registration pitfalls before the 2026 deadline. Jim Macdonell - June 6, 2025 Blogs Medical Device Quality Assurance, Regulatory
osapiens for Medical Devices – BYRD Health Achieves Cloud Assurance Certification, Strengthening Partnership with USDM Life Sciences to Advance Global UDI Compliance BYRD Health earns USDM’s Cloud Assurance Certification, streamlining UDI compliance and ensuring global regulatory readiness for medical devices. Marium Amin - June 3, 2025 News & Events Medical Device Information Technology, Regulatory
Oracle Fusion to Redwood Migration Guide: Timeline, Strategy, and Best Practices Migrate from Oracle Fusion to Redwood with confidence using USDM’s step-by-step strategy, timelines, and compliance-first best practices. Jeff Burton - May 19, 2025 Blogs Medical Device, Pharma 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
EUDAMED Challenges for Medical Device Manufacturers: Future-Proof Your 2025 Compliance Strategy Watch the Replay: Discover how to streamline EUDAMED compliance and UDI registration. Learn from USDM & BYRD Health before the 2026 deadlines hit. Webinars Medical Device Regulatory
