Author(s): Dibyajyoti Saha, Vibhor kumar Jain, Bindu Jain, Roshni Tandey

Email(s): saha.dibyajyoti@gmail.com

DOI: Not Available

Address: Dibyajyoti Saha*, Vibhor kumar Jain, Bindu Jain and Roshni Tandey
School of Pharmacy, Chouksey Engineering College, Lal Khadan Masturi Road, Bilaspur - 495 004, C.G. *Corresponding Author

Published In:   Volume - 1,      Issue - 1,     Year - 2011


ABSTRACT:
Good laboratory practice is an essential part of good manufacturing practice detailed in Schedule M to the Drugs and Cosmetic rule. It involves a number of good practices in the QC laboratory which are to be undertaken to carry out an analysis with a defined degree of accuracy and precision. The importance of GLP is the implementation of GMP detailed in Schedule M cannot be overemphasized. The role of GLP is the development of quality test data, mutual acceptance of data avoids duplication of data, avoids technical barriers to trade and also protection of human health and the environment. The present article highlights important application of GLP in the design of accuracy, precision, reliability etc.


Cite this article:
Dibyajyoti Saha, Vibhor kumar Jain, Bindu Jain, Roshni Tandey. Good Laboratory Practice: Design and Utility. Asian J. Pharm. Tech. 1(1): Jan.-Mar. 2011; Page 01-03.


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