FDA Mandated Global CSV Remediation Case study on FDA Mandated Global CSV Remediation. Diane Gleinser - April 12, 2022 Case Studies Medical Device Information Technology, Quality Assurance, Regulatory
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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? Diane Gleinser - March 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, 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. Erin Christy - March 12, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Safety
Q&A with the FDA on CSV Changes On-demand webinar topic: Q&A with the FDA on CSV Changes. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Quality Assurance, Regulatory
