Evolving Global UDI Product Data Requirements Explore UDI challenges for device manufacturers. Learn to manage regulatory, commercial, and patient safety requirements globally in this on-demand webinar. Webinars Medical Device Clinical, Manufacturing, Quality Assurance, Regulatory
An Introduction to Computer Software Assurance On-demand webinar topic: An Introduction to Computer Software Assurance. Webinars Biotech, CMO, CRO, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory
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... Jay Crowley - April 8, 2022 Blogs Medical Device Manufacturing, Regulatory
Improved UDI Data Integrity with Single-Source-of-Truth Case study on Improved UDI Data Integrity with Single-Source-of-Truth. Jay Crowley - April 5, 2022 Case Studies Medical Device Manufacturing
MDSAP Ready in 4 Months Through Assessment and Remediation Case study on MDSAP Ready in 4 Months Through Assessment and Remediation. Jim Macdonell - April 1, 2022 Case Studies Medical Device Clinical, Manufacturing, Regulatory
Quality System Upgrade to Meet EU MDR and EU IVDR Case study on Quality System Upgrade to Meet EU MDR and EU IVDR. Jay Crowley - March 18, 2022 Case Studies Medical Device Manufacturing, Regulatory
