Remove Article Remove Method Validation Remove Pharmaceutical Manufacturing
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Overview of pharmaceutical quality control steps and implementations

GMPSOP

From starting materials to testing pharmaceutical products coming out of the manufacturing process, quality control is the only function that detects unknown defects early and allows for timely correction. This means that the analytical methods consistently generate true results with precision and accuracy every time.

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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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Concept of validation in pharmaceutical industry

GMPSOP

What is method validation in pharmaceutical industry? Analytical method validation involves demonstrating that the analytical methods used to test the quality of your product are accurate, reliable and reproducible which is critical for ensuring the quality and safety of your products.

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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.