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Optimize cleaning validation in pharmaceutical manufacturing with key strategies for selecting worst-case scenarios, ensuring product safety and efficacy....
Explore the new 2024 Cannabis Flower Ph.Eur Monograph, setting new quality standards for medicinal cannabis from July 1, 2024....
Explore the critical steps of cleanroom qualification and validation within GMP environments, emphasizing the importance of design, operational standards, and...
Discover the essentials of Process Validation Lifecycle with a risk-based approach. Learn how to ensure product integrity from development to...
Explore the classes and regulatory guidelines used in Residual Solvents testing in GMP....
Discover the essentials of Process Validation in GMP, ensuring pharmaceutical quality through scientific and regulatory practices....
Exploring Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) - essential steps in ensuring equipment quality and compliance in...
Explore the key differences of GMP vs GLP and how these practices warrant the highest industry standards....
Explore essential strategies for mitigating risks in temperature-controlled environments, ensuring product stability and safety in pharmaceutical storage....
Learn about all the phases of addressing Out of Specification (OOS) results in the pharmaceutical industry...

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