Pharmaceutical IT & Regulatory Compliance Resources

FDA AI Guidance 2025: What Life Sciences Must Do Now

Explore the FDA’s evolving AI enforcement, new guidance, and what life-science organizations must do to stay compliant with AI in GxP environments.

John Petrakis
- November 17, 2025

Blogs

Medical Device, Pharma

Information Technology, Quality Assurance

How to Leverage USDM’s Vendor Audit of Oracle Supply Chain Management Cloud

Kim Hutchings
- November 6, 2025

Blogs

Biotech, CMO, CRO, Medical Device, Pharma

Manufacturing

The Hidden Costs of Offshore IT Projects in Life Sciences: Why Local Expertise Matters

Discover why offshore IT projects fail in life sciences and how USDM Life Sciences delivers local, compliant, and accountable project success.

John Danese
- October 6, 2025

Blogs

Biotech, Medical Device, Pharma

Information Technology, Quality Assurance

ETM.AI: The AI-Enabled Digital Enterprise Trace Matrix

USDM Life Sciences and Oracle are transforming Enterprise Trace Matrix management with AI-driven compliance built into workflows for continuous audit readiness.

Kim Hutchings
- October 6, 2025

Blogs

Biotech, Pharma

Information Technology, Quality Assurance

AI‑Powered Quality Management for Life Sciences

USDM helps a leading life sciences company transform quality operations with AI-powered Veeva Vault QMS for speed, compliance, and efficiency.

Rathina Govindaswamy
- August 20, 2025

Case Studies

Biotech, Pharma

Clinical, Information Technology, Manufacturing

Join us at Oracle AI World 2025

Join USDM, Apps Associates, and Oracle for an exclusive Life Sciences Lunch event during AI World 2025. Learn how to fast-track regulatory compliance and innovation with Oracle CloudSure.

Darlene Limtiaco
- July 15, 2025

News & Events

Biotech, CMO, CRO, Medical Device, Pharma

Clinical, Information Technology, Manufacturing