Industry Expertise
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.
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.
