How to Align your CSV Program with the FDA’s CSA Approach Blog article topic: How to Align your CSV Program with the FDA’s CSA Approach. Jim Macdonell - April 27, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
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
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
Challenges with EU MDR and IVDR Compliance On-demand webinar topic: Challenges with EU MDR and IVDR Compliance. Webinars Medical Device Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Safety
Cannabis: Compliance in a Rapidly Changing Industry On-demand webinar topic: Cannabis: Compliance in a Rapidly Changing Industry. Webinars Pharma Clinical, Manufacturing, Quality Assurance, Regulatory, Safety
