Pharmaceutical Company Transitions to CSA Model with USDM Expertise Learn how USDM helped a pharmaceutical company achieve greater efficiencies in their validation process through a hybrid CSA model for testing. Sandy Hedberg - July 26, 2022 Case Studies Pharma Regulatory
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
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
Box GxP and Cloud Assurance for FDA Submission Case study on Box GxP and Cloud Assurance for FDA Submission. David Blewitt - April 19, 2022 Case Studies Biotech, Pharma Clinical
SaMD Regulations and Compliant Development Environments Learn about SaMD regulations, QMS implications, and IT development environments. Explore U.S. and EU compliance requirements in this insightful webinar. Webinars Medical Device Clinical, Information Technology
