000			02071pam a2200409 a 4500
999			_c12893 _d12893
001			4904906
005			20210307123039.0
008			940216s1994 nyu b 001 0 eng d
010			_a 94006372
020			_a0824790146 (alk. paper)
040			_aEG-NcFUE _cEG-NcFUE _dEG-NcFUE _erda
050	0	0	_aRA761 _b.H29 1994
060	0	0	_aW1 DR893B v. 64 1994 _aWA 240 H193a 1994
082	0	0	_220 _a614.48 _bH.N.A
100	1		_aHalls, Nigel A., _d1945- _eauthor
245	1	0	_aAchieving sterility in medical and pharmaceutical products / _cNigel A. Halls.
264		1	_aNew York : _bM. Dekker, _c[1994]
264		4	_a©1994.
300			_aiv, 281 pages : _billustrations ; _c23 cm.
336			_2rdacontent _atext
337			_2rdamedia _aunmediated
338			_2rdacarrier _avolume
440		0	_aDrugs and the pharmaceutical sciences ; _vvolume 64
504			_aIncludes bibliographical references and index.
505	0		_aThe Need for SterilitySterility and Sterility AssuranceSterilization by Gamma RadiationSterilization by Saturated SteamDry Heat Sterilization and DepyrogenationSterilization by Ethylene OxideSterilization by FiltrationAseptic ManufactureMaintenance of SterilityParametric Release and Other Regulatory Issues
520			_aDetails the scientific principles underlying the achievement of sterility; examines practical, commonly-used sterilization procedures and the methods available to confirm sterility; and assesses the strengths and limitations of each technology. Regulatory requirements for sterility are defined.
650		0	_aSterilization.
650		0	_aDrugs _xSterilization.
650		2	_aSterilization _xmethods.
650		2	_aDrug Contamination _xprevention & control.
650		2	_aEquipment and Supplies.
856	4	2	_3Publisher description _uhttp://www.loc.gov/catdir/enhancements/fy0647/94006372-d.html
906			_a7 _bcbc _corignew _d1 _eocip _f19 _gy-gencatlg
942			_2ddc _cBK