Q&A: EU MDR Date of Application Readiness Blog article written from the Q&A during the EU MDR Date of Application Readiness webinar. 0 Jay Crowley - April 19, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
USDM’s Guide to 21 CFR Part 11 Blog article topic: USDM’s Guide to 21 CFR Part 11. 0 David Blewitt - April 14, 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? 0 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. 0 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. 0 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. 0 Joseph Cassella - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
