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040			_aAIKTC-KRRC _cAIKTC-KRRC
041			_aENG
082			_a615 _bWEI _2DDC23
100			_aWeinberg, Sandy _93892
245		0	_aGood laborotary practice regulation
250			_a3rd
260			_aNew York _c2005
300			_a244, 23.4*15.8 Pages _bPaperback
440			_aDrugs and the Pharmaceutical Sciences _93678
490			_aSwarbrick, James
520			_aFrom the Publisher Fully updated and revised to include the latest information since publication of the first edition in 1989, the Second Edition of this highly praised reference covers all aspects of the Food and Drug Administration's (FDA) Good Laboratory Practice (GLP) regulations and techniques for implementation. The book details specific standards and general guidelines for the management of efficient and effective research environment. A guide to the current standards and requirements of good laboratory management, the book examines essential theoretical principles for anticipating new and emerging interpretations of GLP in a variety of laboratory settings. Editorial Reviews - Good Laboratory Practice Regulations, Third Edition, Revised and Expanded, Vol. 124 From the Publisher Fully updated and revised to include the latest information since publication of the first edition in 1989, the Second Edition of this highly praised reference covers all aspects of the Food and Drug Administration's (FDA) Good Laboratory Practice (GLP) regulations and techniques for implementation. The book details specific standards and general guidelines for the management of efficient and effective research environment. A guide to the current standards and requirements of good laboratory management, the book examines essential theoretical principles for anticipating new and emerging interpretations of GLP in a variety of laboratory settings. Booknews Discusses the Good Laboratory Practice Regulations promulgated by the US Food and Drug Administration in 1976 and frequently revised since then, how to implement them, why they should be followed even in laboratories not legally subject to them, and how they fit into the larger picture of US and global regulation and practice. Discusses the historical development of the regulations, automated laboratories, computer systems, validation, the FDA's inspection program, and the cybernetic necessity for the regulations. Emphasizes the i
650		0	_910712 _aPHARMACY PRACTICE
856			_uhttps://ndl.iitkgp.ac.in/result?q={%22t%22:%22search%22,%22k%22:%22pharmaceutics%22,%22s%22:[%22DDC=\%22600%3A%3ATechnology\%22%22],%22b%22:{%22filters%22:[]}}
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