Resources

Thought Leadership from Trusted Experts

Thoughts, perspectives, and guidance on the on the challenges and solutions captivating the life sciences industry today. We can help you prepare for tomorrow.

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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

Global UDI Data Management – The New Paradigm

Currently, multiple regulators have or are launching national UDI Databases (US, EU, SFDA, NMPA, KFDA, HSA). Other regulators are following close behind. The new UDI challenge for device manufacturers is creating and submitting the required data to these national databases and maintaining this data – and regulatory compliance – over time.

Webinars

Medical Device

Manufacturing

USDM’s Cloud Assurance Certification is THE Badge of Trust for Life Sciences Companies When Selecting Technology Vendors

Lisa Om
- July 12, 2022

News & Events

Biotech, Medical Device, Pharma

Automate Validation Across Your Tech Stack

WHITE PAPER: In this white paper, we discuss considerations for managing GxP cloud compliance, automating validation and regression testing, evolving your IT infrastructure to utilize a building block approach to minimize compliance burdens, and the benefits of USDM’s Cloud Assurance managed service.