Veeva’s MedTech Summit 2022 | Minneapolis, MN Join USDM's Jay Crowley to discuss the growing UDI landscape, the similarities and differences of various UDI regulations, and their impact on MedTech organizations. Lisa Om - May 17, 2022 News & Events Medical Device Information Technology, Manufacturing, Regulatory
Automating Validation Across Your Tech Stack ON-DEMAND WEBINAR: This webinar will addresses forward-thinking validation and continuous compliance considerations for modern cloud technologies. Webinars Biotech, Medical Device, Pharma Clinical, Information Technology, Quality Assurance, Regulatory
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
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
