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
Mandatory Use of EUDAMED Now Starting Q1 2026 ON-DEMAND WEBINAR: Technical considerations and guidance for managing UDI data to meet the deadline Webinars Medical Device Regulatory
Veeva MedTech 2024 in Austin Join Veeva and USDM at Veeva MedTech Summit in Austin from April 29th to May 1st. Jay Crowley will be speaking on Holistic Data Management. Lisa Om - April 4, 2024 News & Events Medical Device Information Technology, Regulatory
An Update on the FDA’s UDI and GUDID Compliance Requirements ON-DEMAND WEBINAR: An update on the FDA’s requirements and notification activities and aims to answer many of the incoming questions our UDI consultants have received recently. Webinars Medical Device Manufacturing, Regulatory
Continued Confusion and Misinformation about UDI Implementations Feeling confused by UDI implementations? See USDM Life Sciences tips in this blog. Learn more today! Jay Crowley - June 1, 2023 Blogs Medical Device Quality Assurance, Regulatory
Veeva & USDM at Veeva MedTech 2023 in Chicago Join Veeva and USDM at Veeva MedTech Summit in Chicago at May 30 to June 1st. USDM will be speaking. Join us there! Ryan McDonald - March 10, 2023 News & Events Medical Device Information Technology, Regulatory
