News filtered by category

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 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 about the process for ensuring controlled storage conditions, temperature mapping. Discover key equipment considerations. cGMP Consulting can help!

Learn why temperature mapping is vital for FDA-regulated distributors—ensuring compliance, product integrity, and risk protection.

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.

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

Temperature mapping is a Good Manufacturing Practice (GMP) utilized by a variety of industries to capture how temperature is distributed within a space.

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