Industry Expertise
Discover how cGMP Consulting’s validation engineers support GMP compliance through documentation, coordination, execution, and audit-ready processes.
Struggling with test methods and specs? See how cGMP Consulting guides dietary supplement makers to confident compliance with 21 CFR Part 111.
Ensure your gloves meet compliance standards. Explore essential glove testing procedures for GMP certification and safety in manufacturing.
Discover how to build intelligent factories with digital technologies, agile processes, and modular systems. Improve efficiency, sustainability, and adaptability in modern manufacturing.
Learn how to create an effective Periodic Validation Review (PVR) Schedule for qualified equipment and systems
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.
Learn how pharmaceutical aggregation establishes traceability in the supply chain by linking serialized packaging.
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.
Automated cleaning in pharmaceuticals optimizes labor efficiency, ensures consistent results, and enhances safety through PLC monitoring.
