Q&A: EU MDR Date of Application Readiness Blog article written from the Q&A during the EU MDR Date of Application Readiness webinar. Jay Crowley - April 19, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
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
Optimized Use of TraceLink Helps Pharma Company Implement Serialization Case study on Optimized Use of TraceLink Helps Pharma Company Implement Serialization. Erin Christy - April 18, 2022 Case Studies Pharma Information Technology, Regulatory
ERP Validation in 80% Less Time! Case study on ERP Validation in 80% Less Time!. Diane Gleinser - April 17, 2022 Case Studies Medical Device Quality Assurance, Regulatory
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
FDA CBD Enforcement Report Released to Congress Blog article topic: FDA CBD Enforcement Report Released to Congress. Joseph Cassella - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
