000			02925cam a2200421Mu 4500
001			9781315102917
003			FlBoTFG
005			20220509192931.0
006			m d
007			cr cnu---unuuu
008			191207s2019 xx o 000 0 eng d
040			_aOCoLC-P _beng _cOCoLC-P
020			_a9781351593519
020			_a135159351X
020			_a9781315102917 _q(electronic bk.)
020			_a1315102919 _q(electronic bk.)
020			_a9781351593502 _q(electronic bk. : EPUB)
020			_a1351593501 _q(electronic bk. : EPUB)
020			_a9781351593496 _q(electronic bk. : Mobipocket)
020			_a1351593498 _q(electronic bk. : Mobipocket)
035			_a(OCoLC)1130038559
035			_a(OCoLC-P)1130038559
050		4	_aRS200
072		7	_aMED _x071000 _2bisacsh
072		7	_aMMG _2bicssc
082	0	4	_a615.19 _223
100	1		_aNiazi, Sarfaraz, _d1949-
245	1	0	_aHandbook of Pharmaceutical Manufacturing Formulations. _nVolume Three, _pLiquid Products.
250			_aThird edition.
260			_aMilton : _bCRC Press LLC, _c2019.
300			_a1 online resource (457 p.)
500			_aDescription based upon print version of record.
520			_aThe Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Three, Liquid Products is an authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing. With thoroughly revised and expanded content, thisthirdvolume of a six-volume set, compiles data from FDA and EMA new drug applications, patents and patent applications, and other sources of generic and proprietary formulations including author's own experience, to cover the broad spectrum of cGMP formulations and issues in using these formulations in a commercial setting. A must-have collection for pharmaceutical manufacturers, educational institutions, and regulatory authorities, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent. Features: Largest source of authoritative and practical formulations, cGMP compliance guidance and self-audit suggestions Differs from other publications on formulation science in that it focuses on readily scalable commercial formulations that can be adopted for cGMP manufacturing Tackles common difficulties in formulating drugs and presents details on stability testing, bioequivalence testing, and full compliance with drug product safety elements Written by a well-recognized authority on drug and dosage form development including biological drugs and alternative medicines
588			_aOCLC-licensed vendor bibliographic record.
650		7	_aMEDICAL / Pharmacology _2bisacsh
650		0	_aDrugs _xDosage forms.
856	4	0	_3Taylor & Francis _uhttps://www.taylorfrancis.com/books/9781315102917
856	4	2	_3OCLC metadata license agreement _uhttp://www.oclc.org/content/dam/oclc/forms/terms/vbrl-201703.pdf
999			_c126811 _d126811