FDA Mandated Global CSV Remediation Case study on FDA Mandated Global CSV Remediation. Diane Gleisner - April 12, 2022 Case Studies Medical Device Information Technology for Life Science Organizations, Quality Assurance for Life Science Organizations, Regulatory
MDSAP Ready in 4 Months Through Assessment and Remediation Case study on MDSAP Ready in 4 Months Through Assessment and Remediation. Jim Macdonell - April 1, 2022 Case Studies Medical Device Clinical, Manufacturing, Regulatory
Quality System Upgrade to Meet EU MDR and EU IVDR Case study on Quality System Upgrade to Meet EU MDR and EU IVDR. Jay Crowley - March 18, 2022 Case Studies Medical Device Manufacturing, Regulatory
What are Key Performance Indicators for a Life Sciences Project? Blog article topic: What are Key Performance Indicators for a Life Sciences Project? 0 Diane Gleisner - March 14, 2022 Blogs Biotech, Clinical Research Organization, Contract Manufacturing Organization, Medical Device, Pharma Clinical, Information Technology for Life Science Organizations, Manufacturing, Quality Assurance for Life Science Organizations, Regulatory, Research & Development, Safety
Standard Operating Procedures (SOPs) – Best Practices for Emerging Life Sciences Companies Blog article topic: Standard Operating Procedures (SOPs) – Best Practices for Emerging Life Sciences Companies. 0 Erin Christy - March 12, 2022 Blogs Biotech, Clinical Research Organization, Contract Manufacturing Organization, Medical Device, Pharma Quality Assurance for Life Science Organizations, Safety
Q&A with the FDA on CSV Changes On-demand webinar topic: Q&A with the FDA on CSV Changes. 0 Webinars Biotech, Clinical Research Organization, Contract Manufacturing Organization, Medical Device, Pharma Information Technology for Life Science Organizations, Quality Assurance for Life Science Organizations, Regulatory
