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Overview of pharmaceutical quality control steps and implementations

GMPSOP

This article will focus on some of the common activities performed in quality control facilities daily to maintain the expected level of compliance and ensuring product quality. This means that the analytical methods consistently generate true results with precision and accuracy every time. accuracy, precision, etc.)

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Validation master plan (VMP) – when and how to create one?

GMPSOP

If you are in the pharmaceutical business, regulatory authorities mandate that you develop, implement, and periodically review a validation master plan for qualifying your systems, processes, cleaning method, testing methodologies, equipment, facilities, etc. Method validation master plan?

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What are the elements of quality control process in pharmaceuticals

GMPSOP

Validated test method A test method comprehensively describes all procedures used in sample analysis. Analytical test method validation guarantees that your test method is robust enough to provide evidence if your product meets the predetermined product specification or conforms to the failure of a product.