• SHINE SUDEV
• Farsana
• Mohamed.P
• Ameer Suhail.A.K
• Anju Jose

Validation part is the most important and recognized parameter in the cGMPs. The process validation is standardization of the validation documents that has got to be submitted with the submission file for promoting authorization. According to agency (FDA), assurance of product quality springs from careful and general attention to variety of importance factors, including: selection of quality process through in-process and end-product testing. Validation is a concept that has evolved in unite states in 1978.The concept of validation has expanded through the years to embrace a wide range of activities from analytical methods used for the standard management of drug substances and drug product to processed systems for clinical trials, labeling or process control. Validation is founded on, however not prescribed by regulative needs and is best viewed as a very important and integral a part of cGMP.

validation, Importance, Scope, Types

"COMPREHENSIVE STUDY AND REVIEW ON PHARMACEUTICAL VALIDATION", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.6, Issue 6, page no.90-102, June 2019, Available :http://www.jetir.org/papers/JETIR1907L67.pdf

"COMPREHENSIVE STUDY AND REVIEW ON PHARMACEUTICAL VALIDATION", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.6, Issue 6, page no. pp90-102, June 2019, Available at : http://www.jetir.org/papers/JETIR1907L67.pdf