Adapting Computer System Validation to Accommodate Evolving FDA Guidance Blog article topic: Adapting Computer System Validation to Accommodate Evolving FDA Guidance. Sandy Hedberg - April 27, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
Compliant Data Migration Solutions Blog article topic: Compliant Data Migration Solutions. Joseph Cassella - April 26, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
Demystify FDA Compliance for Public Cloud Workloads in Life Sciences Explore best practices for FDA-compliant cloud adoption in life sciences. Learn about workload analysis, compliance management, and secure cloud strategies. Webinars Biotech, CMO, CRO, Medical Device, Pharma Information Technology, 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
Five Tips for Successful Veeva Implementation Blog article topic: Five Tips for Successful Veeva Implementation. Donald Zinn - April 14, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
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
