release of finished products

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srikrupa institute of pharmaceutical analysis

This document is an assignment submitted by Huzaifa Naaz on the topic of releasing finished pharmaceutical products. It discusses requirements for quality control and assurance that must be met before products can be released for distribution and sale. Key aspects covered include testing for purity, potency, and stability to ensure the products meet all specifications.

Education

SRIKRUPA INISTITUTE OF PHARMACEUTICAL SCIENCES
(Approved by AICTE; PCI)
(Affiliated to Osmania University)
ASSIGNMENT ON
RELEASE OF FINISHED PRODUCTS
SUBMITTED BY
HUZAIFA NAAZ

Analytical method validation is a process of documenting/ proving that an analytical method provides analytical data acceptable for the intended use.After the development of an analytical procedure, it is must important to assure that the procedure will consistently produce the intended a precise result with high degree of accuracy. The method should give a specific result that may not be affected by external matters. This creates a requirement to validate the analytical procedures. The validation procedures consists of some characteristics parameters that makes the method acceptable with addition of statistical tools.

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