000			02079cam a22003854a 4500
001			4689
003			BD-DhEWU
005			20180114110321.0
008			080809s2003 nyu g b 001 0 eng d
010			_a 2002035159
020			_a0824708911 (alk. paper)
020			_a9780824708917
035			_a(OCoLC)50809017
040			_aDLC _cDLC _dDLC _dBD-DhEWU _beng
041			_aeng
050	0	0	_aR850 _b.G66 2003
082	0	4	_a615.19 _bGOO 2003
245	0	0	_aGood laboratory practice regulations / _cedited by Sandy Weinberg.
250			_a3rd ed.
260			_aNew York : _bMarcel Dekker, _c2003.
300			_ax, 244 p. ; _c23 cm.
440		0	_aDrugs and the pharmaceutical sciences ; _vv. 124 _921405
504			_aIncludes bibliographical references (p. 229-237) and index.
505			_tTOC _aHistorical Perspective, Jean M. Taylor and Gary C. SteinFDA/ GLP Regulations, Wendell A. PetersonApplying 21 CFR Part 11 to the Laboratory Environment, Sandy WeinbergThe Good Automated Laboratory Practices, Gerald J. Whartenby, Paul L. Robinson, and Sandy WeinbergImplementing GLP's in a Non-GLP Analytical Laboratory, Stephanie A. OlexaComputer Systems Validation, Sandy WeinbergThe FDA's GLP Inspection Program, George W. JamesThe Future, Sandy WeinbergBibliographyIndex
520			_aSummary: Covers all aspects of the Food and Drug Administration's (FDA), Good Laboratory Practice (GLP) regulations and techniques for implementation. This book details standards and general guidelines for the management of research environment. It examines theoretical principles for anticipating interpretations of GLP in a variety of laboratory settings
526			_aPharmacy
590			_aSagar Shahanawaz
650		0	_aMedical laboratories _xQuality control. _98612
650		0	_aPharmaceutical technology. _98613
700	1		_aWeinberg, Sandy, _d1950- _98614
856	4	2	_3Publisher description _uhttp://www.loc.gov/catdir/enhancements/fy0647/2002035159-d.html
856	4	0	_3E-book Fulltext _uhttp://lib.ewubd.edu/ebook/4689
942			_2ddc _cTEXT _02
999			_c4689 _d4689
999			_c4689 _d4689