000 01832cam a22003014i 4500
999 _c2107
_d2107
001 12962874
005 20190718131523.0
008 021010s2003 nyu b 001 0 eng
020 _a0824708911 (alk. paper)
040 _aDLC
_cDLC
_dDLC
_erda
082 0 0 _a615.19072
_221
_bG
245 0 0 _aGood laboratory practice regulations /
_cedited by Sandy Weinberg.
250 _aThird edition.
264 1 _aNew York :
_bMarcel Dekker,
_c2003.
300 _ax, 244 pages. ;
_c23 cm.
336 _2rdacontent
_atext
337 _2rdamedia
_aunmediated
338 _2rdacarrier
_avolume
440 0 _aDrugs and the pharmaceutical sciences ;
_vv. 124
504 _aIncludes bibliographical references (p. 229-237) and index.
505 0 _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 Weinberg Bibliography Index
520 _aCovers 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
650 0 _aMedical laboratories
_xQuality control.
650 0 _aPharmaceutical technology.
700 1 _aWeinberg, Sandy,
_d1950-
_eeditor.
_98603
856 _3Abstract
_uhttp://repository.fue.edu.eg/xmlui/handle/123456789/1542
942 _cBK
_2ddc