The Evolving Global Medical Device Data Imperative Device manufacturers are facing complex challenges when it comes to assessing, planning, and executing UDI regulations. 0 Jay Crowley - May 1, 2022 Blogs Medical Device Manufacturing
GxP Expertise for Program and Project Management Rather than spending too much time on project and program management yourself, turn to the experts. 0 Erin Christy - April 27, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
Adapting Computer System Validation to Accommodate Evolving FDA Guidance Blog article topic: Adapting Computer System Validation to Accommodate Evolving FDA Guidance. 0 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. 0 Joseph Cassella - April 26, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology
Demystify FDA Compliance for Public Cloud Workloads in Life Sciences ON DEMAND WEBINAR: Demystify FDA Compliance for Public Cloud Workloads in Life Sciences. 0 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
