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. 1 Webinars Medical Device Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory
EU MDR Date of Application Readiness On-demand webinar topic: EU MDR Date of Application Readiness. 1 Webinars Medical Device Clinical, Information Technology, Manufacturing
Evolving Global UDI Product Data Requirements On-demand webinar topic: Evolving Global UDI Product Data Requirements. 0 Webinars Medical Device Clinical, Manufacturing, Quality Assurance, Regulatory
Challenges with EU MDR and IVDR Compliance On-demand webinar topic: Challenges with EU MDR and IVDR Compliance. 0 Webinars Medical Device Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Safety
Global UDI Database: What if a Medical Device is Discontinued? At some point in the future when a product is no longer distributed, the medical device company will need to... 0 Jay Crowley - April 8, 2022 Blogs Medical Device Manufacturing, Regulatory
Master Data Management and Validation to Meet Global Requirements Case study on Master Data Management and Validation to Meet Global Requirements. Jay Crowley - April 7, 2022 Case Studies Medical Device Information Technology, Quality Assurance, Regulatory
