Veeva’s MedTech Summit 2022 | Minneapolis, MN Join USDM's Jay Crowley to discuss the growing UDI landscape, the similarities and differences of various UDI regulations, and their impact on MedTech organizations. 0 Lisa Om - May 17, 2022 News & Events Medical Device IT, Manufacturing, Regulatory
The Evolving Global Medical Device Data Imperative Device manufacturers are facing complex challenges when it comes to assessing, planning, and executing UDI regulations. 0 Jay Crowley - May 1, 2022 Blogs Medical Device Manufacturing
Most Misunderstood and Misapplied UDI Requirements Blog article topic: Most Misunderstood and Misapplied UDI Requirements. 0 Jay Crowley - April 21, 2022 Blogs Medical Device Manufacturing, Regulatory
How to Comply with Saudi Arabia UDI Requirements On-Demand Webinar Topic: How to Comply with Saudi Arabia UDI Requirements. 0 Webinars Medical Device Clinical, IT, Manufacturing, QA, Regulatory
UDI Registration in EUDAMED – Why and How to Use It Now On-demand webinar topic: UDI Registration in EUDAMED – Why and How to Use It Now. 0 Webinars Medical Device Clinical, IT, Manufacturing, QA, Regulatory
How to Maximize Your GxP Use of the Public Cloud On-demand webinar topic: How to Maximize Your GxP Use of the Public Cloud. 0 Webinars Biotech, Medical Device, Pharma Clinical, IT, Manufacturing, QA, Regulatory
