GMPSOP

SEPTEMBER 27, 2023

Cleaning validation verifies that the cleaning procedure can consistently and significantly reduce the amount of active ingredients, excipients, and cleaning agents to a concentration within the acceptance limit. Why is cleaning validation required? If it is not, analytical method validation is required.

Method Validation 98

Method Validation Documentation Pharmaceutical Manufacturing Dosage 98

GMPSOP

OCTOBER 26, 2022

Additionally, validation includes continuous monitoring and re-evaluation to ensure that the product or process remains in compliance with the established requirements. By implementing robust validation protocols, pharmaceutical companies can ensure that their products are safe, effective, pure and of the highest quality.

Documentation 52

Documentation Method Validation Packaging Pharmaceutical Companies 52

GMPSOP

OCTOBER 28, 2023

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.

Documentation 52

Documentation Method Validation Packaging Data Entry 52