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999 _c16892
_d16892
001 4471793
005 20200924110812.0
008 960701s1997 nyua b 001 0 eng c
010 _a 96031653
020 _a0824797701 (acidfree paper)
040 _aDNLM/DLC
_cDLC
_dDLC
043 _an-us---
050 0 0 _aRS 189
_b.W57 1997
060 1 0 _aW1 DR893B v.78 1997
_aQV 771 W732g 1997
082 0 0 _a615/.19/0685
_220
100 1 _aWillig, Sidney H.
_d1919-
_939009
245 1 0 _aGood manufacturing practices for pharmaceuticals :
_ba plan for total quality control /
_cSidney H. Willig, James R. Stoker
250 _a4th ed., rev. and expanded.
260 _aNew York :
_bMarcel Dekker,
_c1997
300 _ax, 496 p. :
_bill. ;
_c24 cm.
440 0 _aDrugs and the pharmaceutical sciences ;
_vv. 78
_923033
504 _aIncludes bibliographical references and index.
650 0 _aPharmaceutical industry
_xQuality control.
_939010
650 0 _aDrugs
_xStandards
_zUnited States.
_939011
650 1 2 _aDrugs
_xstandards
_zUnited States.
_939012
650 2 2 _aDrug Industry
_xstandards
_zUnited States.
_939013
650 2 2 _aTechnology, Pharmaceutical
_xstandards
_zUnited States.
_939014
650 2 2 _aQuality Control.
_939015
650 2 2 _aLegislation, Drug
_zUnited States.
_939016
700 1 _aStoker, James R.
_939017
906 _a7
_bcbc
_corignew
_d1
_eocip
_f19
_gy-gencatlg
942 _2lcc
_cBK