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Discover how cGMP Consulting’s validation engineers support GMP compliance through documentation, coordination, execution, and audit-ready processes.

Explore what it takes to move from preclinical to clinical, with a focus on cGMP readiness and key challenges to be aware of for a successful transition.

Key questions to evaluate GMP certification readiness, spot gaps, and build a stronger quality system for FDA-regulated industries.

Learn how six key trends are reshaping dietary supplement manufacturing and 21 CFR Part 111 compliance across the industry.

Learn how a risk-based approach streamlines facilities, utilities, and equipment qualification for smarter, compliant pharmaceutical manufacturing.

Ensure compliance with controlled room temperature qualification and temperature mapping for warehouses, freezers, and incubators.

Ensure compliance through proper facility, utility, and equipment qualification. Learn about IQ, OQ, PQ, and best practices for pharmaceutical manufacturing.

Learn why equipment requalification is essential for maintaining FDA compliance and operational efficiency.

Learn the key steps and best practices to qualify sterile fill line equipment and ensure compliance.

Discover proven data integrity practices for CQV to maintain compliance in equipment qualification processes.

Optimize your equipment for GMP compliance. Our guide covers qualification steps to ensure performance, reliability, and regulatory standards

Discover how to build intelligent factories with digital technologies, agile processes, and modular systems. Improve efficiency, sustainability, and adaptability in modern manufacturing.

Discover what a Periodic Validation Review (PVR) is, how it's conducted, and how often it should be performed to ensure ongoing compliance and system control.

Cleanrooms are highly controlled spaces where pharmaceuticals are produced. Cleaning is the key element of contamination control.