Remove Data Entry Remove Information Remove Method Validation
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Typical GMP documentation in a quality control laboratory

GMPSOP

– Documentation of all reagents and materials used in the laboratory, including lot numbers, expiration dates, and supplier information. Data management policy : This policy governs activities for data entry, storage, and retrieval to ensure the integrity of laboratory results.

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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.

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Overview of GLP requirements on everyday laboratory operations

GMPSOP

– Record or capture all generated raw data directly, promptly and legibly. – Use traceable data sheets or sequentially numbered notebooks. – Date and sign or initial data entries on the day of entry. – Test method validation protocols, data and reports – Other records and data i.