GxP Expertise for Program and Project Management Rather than spending too much time on project and program management yourself, turn to the experts. 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. Sandy Hedberg - April 27, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Information Technology, Regulatory
List of Supported Regulations Blog article topic: List of Supported Regulations. Diane Gleinser - April 27, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory
How to Align your CSV Program with the FDA’s CSA Approach Blog article topic: How to Align your CSV Program with the FDA’s CSA Approach. Jim Macdonell - April 27, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Regulatory, Safety
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
Clinical Compliance as a Service Learn how USDM reduced clinical study time and costs for a $16B pharmaceutical company with managed services for EDC, IRT, and ePRO systems. Erin Christy - April 26, 2022 Case Studies Pharma Information Technology, Regulatory
