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Abstract

OVERVIEW OF PHARMACEUTICAL PROCESS VALIDATION

*Rahul Kumar Shah, Vivek Verma, Sunayana Tyagi and Dr. Mojahid Ul Islam

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Abstract

In direction to increase the value of pharmaceutical products, validating the process was established now the twentieth century. Over the last 50 years, the validation idea has evolved from analytical procedure used to control pharmaceutical compounds to computer system studies. Verification is the ability of making and performing the phases that have been designed, as well as the documents. Validating the process focuses on procedure project basics and keeping procedure mechanism through commercialization, as well as communicating that maintaining process. It also emphasize the character of objectives processes and statistically apparatuses as well as examines, information, exposure, and control of variable, and also provides guarantee of value uniformity during the life span of product. Verification is an important aspect of quality assurance. In recent years, verification has taken on a greater significance. The article provides an overview and broad introduction to procedure verification in the medical industrial procedure, as well as its significance.

Keywords: Process verification, GMP, Correlation study.


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