Quality Archives

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

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

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 USDM at RAPS Convergence 2025

Join USDM and BYRD Health at RAPS Convergence 2025 to explore EUDAMED compliance, UDI strategies, and MDR/IVDR readiness. Visit booth #537 or register for our workshop.

Darlene Limtiaco
- July 16, 2025

News & Events

Medical Device

Manufacturing, Quality Assurance, Regulatory, Safety

Join USDM at BoxWorks 2025

Join USDM at BoxWorks 2025 to explore AI-driven content management excellence with compliance built-in. Power smarter, compliant content management for life sciences.

Darlene Limtiaco
- July 14, 2025

News & Events

Biotech, CMO, CRO, Medical Device, Pharma

Clinical, Information Technology, Quality Assurance

Join USDM at the Blue Mountain Summit 2025

Join USDM at Blue Mountain Summit 2025 to explore digital compliance strategies, asset management innovation, and GMP excellence for life sciences.

Darlene Limtiaco
- July 14, 2025

News & Events

Biotech, CMO, CRO, Medical Device, Pharma

Information Technology, Manufacturing, Quality Assurance