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The Model Context Protocol (MCP) in Life Sciences

Discover how the Model Context Protocol (MCP) is transforming AI in life sciences—from automating quality operations to powering secure clinical decision support. Learn how to govern and secure MCP for compliance with HIPAA, 21 CFR Part 11, and GxP.

Brian Rankin
- July 10, 2025

Blogs

Biotech, Medical Device, Pharma

Information Technology

The EU AI Act Is Here: What Life Sciences Companies Need to Know Now

The EU AI Act is here. Learn what life sciences companies must do now to ensure compliance, avoid penalties, and stay ahead in a rapidly evolving regulatory landscape.

John Petrakis
- July 9, 2025

Blogs

Biotech, Medical Device, Pharma

Clinical, Information Technology

EUDAMED Compliance: Your Most Pressing Questions—Answered

Get expert answers to top EUDAMED compliance questions and learn how to avoid costly registration pitfalls before the 2026 deadline.

Jim Macdonell
- June 6, 2025

Blogs

Medical Device

Quality Assurance, Regulatory

Evaluating Google Agentspace for Life Sciences

Discover 10 key factors life sciences must assess when adopting Google Agentspace for secure, compliant AI integration.

John Petrakis
- May 22, 2025

Blogs

Information Technology, Regulatory

Oracle Fusion to Redwood Migration Guide: Timeline, Strategy, and Best Practices

Migrate from Oracle Fusion to Redwood with confidence using USDM’s step-by-step strategy, timelines, and compliance-first best practices.

Hovsep Kirikian
- May 19, 2025

Blogs

Medical Device, Pharma

Information Technology

Security Over Speed: Applying J.P. Morgan’s Cyber Risk Mandate to Life Sciences Vendors

Why life sciences must prioritize security over speed—and how smart TPRM strategies protect data, compliance, and patient safety.

Brian Rankin
- May 2, 2025

Blogs

Biotech, CMO, CRO, Medical Device, Pharma

Clinical, Information Technology