000 01471pam a2200421 a 4500
999 _c12895
_d12895
001 1544903
005 20210307124409.0
008 911217s1992 nyua b 001 0 eng d
010 _a 91046914
020 _a0824785940
040 _aEG-NcFUE
_cEG-NcFUE
_dEG-NcFUE
_erda
043 _an-us---
050 0 0 _aRS189
_b.W57 1991
060 _aW1 DR893B v. 52
_aQV 771 W732g
082 0 0 _220
_a615.190685
_bW.S.G
100 1 _aWillig, Sidney H.,
_d1919-
_eauthor
245 1 0 _aGood manufacturing practices for pharmaceuticals :
_ba plan for total quality control /
_cSidney H. Willig, James R. Stoker.
250 _aThird edition
264 1 _aNew York :
_bM. Dekker,
_c[1992]
264 4 _a©1992.
300 _axvi, 268 pages :
_billustrations ;
_c24 cm.
336 _2rdacontent
_atext
337 _2rdamedia
_aunmediated
338 _2rdacarrier
_avolume
440 0 _aDrugs and the pharmaceutical sciences ;
_vvolume 52
504 _aIncludes bibliographical references and index.
650 0 _aPharmaceutical industry
_xQuality control.
650 0 _aDrugs
_xStandards
_zUnited States.
650 2 _aDrug Industry
_xstandards
_zUnited States.
650 2 _aDrugs
_xstandards.
650 2 _aLegislation, Drug
_zUnited States.
650 2 _aQuality Control.
700 1 _aStoker, James R.
_ejoint author
906 _a7
_bcbc
_corignew
_d1
_eocip
_f19
_gy-gencatlg
942 _2ddc
_cBK