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Tag Archives: Process validation

Process Validation of Terbinafine Hydrochloride Tablets and Blend

Kullayappa C*, Naresh G, Muneer S, Hindustan Abdul Ahad  Department of Pharmaceutics, Balaji College of Pharmacy, Ananthapuramu, AP, India Abstract Quality is the primordial intention for process validation is the means of ensuring and providing documentary evidence that processes within their specified design parameters are capable of repeatedly and reliably producing a finished product of required quality. In this study ... Read More »

Process Validation of Aspirin 75 mg Tablets

C. Iniya 1, A. Chenthilnathan1* and V. Vidyasagar2  1Department of Pharmaceutical Chemistry, Manonmaniam Sundaranar University, Tirunelveli–627 012, Tamil Nadu, India. 2Surien Pharmaceuticals (P) Ltd., Chennai–600 122, Tamil Nadu, India. Received: 8 May 2014, Accepted: 29 June 2014, Published Online: 18 July 2014 Abstract Process validation is the means of ensuring and providing documentary evidence that processes within their specified design parameters ... Read More »

A Review on Process Validation of Pharmaceutical Manufacturing Processes

Author Details B. Venkateswara Reddy*, K. Navaneetha, B. Rashmitha, P. Sandeep Department of Pharmaceutics, St.Paul’s College of Pharmacy, Turakayamjal(V), Hayath Nagar(M), Ranga Reddy Dist-501510, A.P, India. Abstract Pharmaceutical Process Validation is the most important and recognized parameters of CGMPs. The requirement of process validation appears of the quality system (QS) regulation. The goal of a quality system is to consistently produce ... Read More »

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