000			01378cam a2200397 a 4500
005			20150712005455.0
008			960701s1997 nyua b 001 0 eng d
010			_a 96031653
020			_a0824797701
040			_aDNLM/DLC _beng _cDLC _dDLC
043			_an-us---
050	0	0	_aRS189 _b.W57 1997
060	1	0	_aW1 DR893B v.78 1997 _aQV 771 W732g 1997
082	0		_a615.190685 _220
084			_a615.190685 _bW.S
100	1		_aWillig, Sidney H., _d1919-
245	1	0	_aGood manufacturing practices for pharmaceuticals _h[Book :] _ba plan for total quality control / _cSidney H. Willig, James R. Stoker.
250			_a4th ed., rev. and expanded.
260			_aNew York : _bMarcel Dekker, _cc1997.
300			_ax, 496 p. : _bill.; ; _c24 cm.
440		0	_aDrugs and the pharmaceutical sciences ; _vv. 78
504			_aIncludes bibliographical references and index.
521			_aAll Ages.
650		0	_aPharmaceutical industry _xQuality control.
650		0	_aDrugs _xStandards _zUnited States.
650	1	2	_aDrugs _xstandards _zUnited States.
650	2	2	_aDrug Industry _xstandards _zUnited States.
650	2	2	_aTechnology, Pharmaceutical _xstandards _zUnited States.
650	2	2	_aQuality Control.
650	2	2	_aLegislation, Drug _zUnited States.
700	1		_aStoker, James R.
866		0	_94 _av.78;()1997
001			0000019760
003			0000
942			_cBK
999			_c52209 _d52209