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Cleaning validation protocol for pharmaceutical industry

GMPSOP

However, you must validate the condition and efficacy of their use by conducting trials. Cleaning validation, including analytical method validation, should be conducted for the new product. If it is not, analytical method validation is required. Additional documents included each month.

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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.