000			02264pam a2200433 i 4500
005			20250919122226.0
008			180605s2017 flua b 001 0 eng
020			_a9781482258905 (alk. paper) _cRM640.93
039		9	_a201806111511 _bfida _y06-05-2018 _zruzini
040			_aDNLM _beng _erda _cDNLM _dUKM _erda
090			_aQV778.G646 2017 9
090			_aQV778 _b.G646 2017 9
245	0	0	_aGood design practices for GMP pharmaceutical facilities / _cedited by Terry Jacobs, Andrew A. Signore.
250			_aSecond edition.
264		1	_aBoca Raton : _bCRC Press/Taylor & Francis Group, _c2017.
264		4	_c©2017.
300			_axviii, 516 pages : _billustrations ; _c24 cm.
336			_atext _2rdacontent
337			_aunmediated _2rdamedia
338			_avolume _2rdacarrier
490	1		_aDrugs and the pharmaceutical sciences ; _vv. 214
500			_aPreceded by: Good design practices for GMP pharmaceutical facilities / Andrew A. Signore, Terry Jacobs. Boca Raton : Taylor & Francis, 2005.
504			_aIncludes bibliographical references and index.
505	0		_aPharmaceutical industry profile -- Current good manufacturing practices -- Legacy facility master planning -- Architectural design issues -- Facility utility systems -- High purity water -- Commissioning, qualification, and validation -- Process engineering -- Oral solid dosage facilities -- Continuous oral solid dose processing -- Sterile manufacturing facilities -- Biotechnology facilities -- Codes and standards -- Containment technology -- Occupational health and safety -- Sustainability -- QA/QC laboratories and related support spaces -- Packaging and warehousing.
650		2	_aTechnology, Pharmaceutical.
650		2	_aFacility Design and Construction.
650		2	_aQuality control.
700	1		_aJacobs, Terry _c(Architect), _eeditor.
700	1		_aSignore, Andrew A., _eeditor.
830		0	_aDrugs and the pharmaceutical sciences ; _vv. 214.
907			_a.b16595944 _b2019-11-12 _c2019-11-12
942			_c01 _n0 _kQV778.G646 2017 9
914			_avtls003634738
990			_afn
991			_aFakulti Farmasi, KKL
998			_ad _b2018-05-06 _cm _da _feng _gflu _y0 _z.b16595944
999			_c627981 _d627981