ABOUT AUTHORS:
Ghodke D.V*, Bhusnure O.G, Kulkarni A.A
Department Of Quality Assurance in Maharashtra College of M .Pharmacy Nilanga.* Dist –Latur
Department Of Medicinal chemistry in Maharashtra College of Pharmacy Nilanga, Dist –Latur
*ghodke.deepa@gmail.com
ABSTRACT
Pharma Industry is facing growing demands for increased productivity and reduced manufacturing costs and also has to meet the evolving need for higher quality standards and higher drug expectations. In traditional approach quality of the raw material attributes both physically and chemically testing was done by off-line process. The application of Process Analytical Technology in pharmaceutical production checks the quality at-line, in-line or on-line thereby decreasing the chances of contamination and cross contamination. Implementation of Process Analytical Technology to pharma industry increased process understanding and continuous improvement also improve regulatory compliance. PAT involves the use of different technologies and tools to build quality into the products. Effective PAT implementation is based on detailed, science-based understanding of the physical, chemical and mechanical properties of all elements of the proposed drug product. In this article, Process Analytical Technology has been introduced its application different tools have been discussed to ensures quality of the pharmaceutical products.
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