Trustworthy, Rapid Remediation to Address FDA 483 Warnings Case study on Trustworthy, Rapid Remediation to Address FDA 483 Warnings. Diane Gleinser - April 18, 2022 Case Studies Biotech 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
Virtual Audits and Inspections On-demand webinar topic: Virtual Audits and Inspections. 1 Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Manufacturing, Quality Assurance, Regulatory, Safety
Validation of SharePoint for GxP Content Management Solution Case study on Validation of SharePoint for GxP Content Management Solution. Erin Christy - April 12, 2022 Case Studies Biotech Research & Development
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
