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
Is There a Checklist for GCP Audits? Blog article topic: Is There a Checklist for GCP Audits? Bob Lucchesi - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
How Do Life Science Companies Qualify Vendors and Software? Automated equipment & systems used by companies are supplied by vendors & are purchased off-the-shelf (OTS). They should audit the vendors development. David Blewitt - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Safety
Five Tips for Successful Veeva Implementation Blog article topic: Five Tips for Successful Veeva Implementation. Donald Zinn - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
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
Virtual Audits and Inspections Explore how virtual audits streamline vendor qualification and regulatory compliance. Learn about technologies enabling efficient remote assessments. Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Safety
