Critical vs. Non-Critical GxP Applications Tips for maintaining quality during transitions of software systems. Sandy Hedberg - August 29, 2022 Blogs Biotech, Medical Device, Pharma Information Technology
Five Tips for GxP Vendor Qualification Blog article topic: A practical guide to make a new technology purchase decision David Blewitt - August 19, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
Q&A: EU MDR Date of Application Readiness Blog article written from the Q&A during the EU MDR Date of Application Readiness webinar. Jay Crowley - April 19, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
FDA CBD Enforcement Report Released to Congress Blog article topic: FDA CBD Enforcement Report Released to Congress. Joseph Cassella - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
Work Faster and Smarter in Biotech Quality Management Discover how Box, ComplianceQuest, and USDM simplify quality management with bundled solutions. Save time, reduce costs, and streamline workflows. Webinars Biotech Information Technology, Quality Assurance
How to Get Results on Regulated Projects with Virtual Teams Learn best practices for managing virtual workforces in regulated environments. Maintain business continuity and compliance with expert insights and tools. Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Quality Assurance, Research & Development
