Process Validation in Pharma: Explained for Modern Manufacturers

February 24, 2026
Lisa Om

Learn how process validation works in pharma, from PPQ and equipment validation to controls, benefits, and modern digital validation approaches used today.

Rethinking Workflow Design in Quality IT: The Untapped Opportunity for Operational Agility

January 22, 2026
Vega Finucan

Discover how life sciences organizations can overcome workflow fragmentation with smarter architecture. Learn why design—not just automation—unlocks scalable compliance and faster outcomes.

What are GxP Validation Processes and How Do They Work

January 20, 2026
Lisa Om

Understand the GxP validation process, key steps, challenges, and trends shaping compliant systems across regulated industries today.

Defining GxP Compliance: Best Practices, Benefits, and More

January 3, 2026
Lisa Om

Learn what GxP compliance is, why it matters, key requirements, affected industries, and best practices. Plus how GxP is evolving for the future.

Beyond ITSM: ServiceNow as the Compliance Engine for Life Sciences

December 4, 2025
Lisa Om

USDM’s Compliant Contact Center delivers validated, 21 CFR Part 11 workflows on ServiceNow—automating intake, triage, and reporting for life sciences teams.

Transforming Regulated ITSM with ProcessX — A Scalable Compliance Engine

October 10, 2025
Lisa Om

Life sciences leader cuts compliance time by 75%, eliminates 4,200 redundant CMDB records, and builds scalable, audit-ready ITSM with ProcessX on ServiceNow.