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
Single Sign-on Significantly Improves Security and Usability Blog article topic: Single Sign-on Significantly Improves Security and Usability. 0 Lisa Om - April 7, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
DevOps Framework Blog article topic: DevOps Framework. 0 Stepheni Norton - April 7, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
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
How to Leverage USDM’s Vendor Audit of Oracle Supply Chain Management Cloud Blog article topic: How to Leverage USDM’s Vendor Audit of Oracle Supply Chain Management Cloud. 0 Kim Hutchings - April 6, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Manufacturing
Top Considerations for Implementing a GxP Content Management System Advice for startups companies in life sciences 0 Erin Christy - April 5, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
