Q&A: UDI Registration in EUDAMED Blog article written from the Q&A during the UDI Registration in EUDAMED webinar. Jay Crowley - January 29, 2022 Blogs Medical Device Regulatory, Safety
Medical Device Company Updates 450 QMS SOPs in time for EU MDR Case study on Medical Device Company Updates 450 QMS SOPs in time for EU MDR. Jim Macdonell - January 21, 2022 Case Studies Medical Device Regulatory, Safety
Auditing-as-a-Service Delivered 80% More Efficient Audits Case Study: USDM revamps antiquated auditing process to save customer’s time and money Bob Lucchesi - January 18, 2022 Case Studies Biotech Quality Assurance, Safety
EU MDR Date of Application Readiness Guide Learn how to navigate EU MDR compliance for medical devices. Understand key deadlines, classification rules, vigilance, and post-market surveillance. Download now! Jay Crowley - January 17, 2022 White Papers Medical Device Clinical, Manufacturing, Quality Assurance, Regulatory, Research & Development, Safety
Is it Acceptable to Push Back if You Disagree with a Notice of Violation or 483? Blog article topic: Is it Acceptable to Push Back if You Disagree with a Notice of Violation or 483? Diane Gleinser - January 13, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
Benefits of Pharmaceutical Serialization Blog article topic: Benefits of Pharmaceutical Serialization. Jim Macdonell - January 9, 2022 Blogs Pharma Regulatory, Safety
