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
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
USDM Life Sciences at the American Medical Device Summit Join us for a quality and regulatory workshop presented by USDM’s Jay Crowley and Hovsep Kirikian on October 2. Michelle Gardner - August 14, 2024 News & Events Medical Device Manufacturing, Regulatory
RAPS Convergence 2024 Lisa Om - August 11, 2024 News & Events Medical Device Manufacturing, Regulatory
Q&A: Mandatory Use of EUDAMED Now Starting Q1 2026 Jay Crowley and Lionel Tussau help make medical device manufacturers aware of key dates, requirements, and regulatory implications. Jay Crowley - July 2, 2024 Blogs Medical Device Manufacturing, Regulatory
