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THE ROLE OF REGULATORY GMP AUDIT IN PHARMACEUTICAL COMPANIES
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Keywords

Auditing, Regulatory aspect, FDA, Audit program, GMP components, Importance, Purpose and procedure of an audit.

How to Cite

Kumar, S. ., Tanwar, D. ., & Arora, N. . (2013). THE ROLE OF REGULATORY GMP AUDIT IN PHARMACEUTICAL COMPANIES. International Journal of Research and Development in Pharmacy & Life Sciences, 2(4), 493-498. Retrieved from https://ijrdpl.com/index.php/ijrdpl/article/view/296

Abstract

The goal of an audit is to express an opinion on the person, organization, system etc. in question, under evaluation based on work done on a test basis. Audits are performed to ascertain the validity and reliability of information; also to provide an assessment of a system's internal control. A company that makes medications today must be able to prove that it does so with absolute reliability, under optimal secure conditions, and with extreme uniformity to allow for exact reproduction. Pharmaceutical auditing expertise includes writing and review of validation policies, guidelines and SOP from design qualification to performance qualification steps.

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