000			03270nam a22003734a 4500
001			ebr10296483
003			CaPaEBR
006			m u
007			cr cn|||||||||
008			080303s2009 njua sb 001 0 eng
010			_z 2008009573
016	7		_z101467523 _2DNLM
020			_z9780470056097 (cloth)
020			_z0470056096 (cloth)
040			_aCaPaEBR _cCaPaEBR
035			_a(OCoLC)352829614
050	1	4	_aRM301.8 _b.F67 2009eb
082	0	4	_a615/.1 _222
245	0	0	_aFormulation and analytical development for low-dose oral drug products _h[electronic resource] / _cedited by Jack Zheng.
260			_aHoboken, N.J. : _bJohn Wiley & Sons, _cc2009.
300			_axxiii, 461 p. : _bill.
504			_aIncludes bibliographical references and index.
505	0		_aAn overview / Jack Y. Zheng -- Challenges and strategies in formulation development of oral solid low-dose drug products / Jack Y. Zheng -- Particle size of drug substance and product content uniformity: theoretical considerations / Kevin C. Johnson -- Development of low-dose formulations using fluidized bed granulation / J. Joe Zhou, and Ralph Lipp -- Development of low-dose solid oral formulations using wet granulation / Ahmad Almaya -- Challenges in development and scale-up of low dose drug products by dry granulation: a case study / Mary T. Am Ende ... [et al.] -- Development of low-dose solid oral tablets using direct compression / Jack Y. Zheng and Robert L. Ternik -- Reduction of particle size of drug substance for low-dose drug products / Christopher L. Burcham ... [et al.] -- Function, quality, and regulations of pharmaceutical excipients for oral solid dosage forms / Jack Y. Zheng --
505	0		_aAnalytical method development: challenges and solutions for low-dose oral dosage forms / Beverly Nickerson ... [et al.] -- In vitro dissolution testing and method development / Vivian A. Gray, Jack Y. Zheng, and Norman N. Sesi -- Analysis of physical transformation of API during manufacture and storage / Gregory A. Stephenson -- Physical characterization tests for drug substances used in low-dose formulations / Ronald G. Lacocca -- An excipient library approach to analytical development for low-dose, solid oral dosage form drug products / Qing Chang ... [et al.] -- Cleaning verification for highly potent compounds / Brian W. Pack -- Containment challenges and strategies for potent compounds in the pharmaceutical industry / Victoria Cathcart, Sarah Jones, Beverly Nickerson -- Sample handling and containment in analytical testing laboratories / David Pattavina, Nancy Sage, Beverly Nickerson -- Regulatory considerations in the development of low-dose solid oral drug products / Ravi S. Harapanhalli.
533			_aElectronic reproduction. _bPalo Alto, Calif. : _cebrary, _d2013. _nAvailable via World Wide Web. _nAccess may be limited to ebrary affiliated libraries.
650		0	_aDrugs _xDose-response relationship.
650		0	_aDrugs _xDosage.
650		0	_aOral medication.
650		0	_aDrug development.
655		7	_aElectronic books. _2local
700	1		_aZheng, Jack.
710	2		_aebrary, Inc.
856	4	0	_uhttp://site.ebrary.com/lib/rucke/Doc?id=10296483 _zAn electronic book accessible through the World Wide Web; click to view
999			_c77341 _d77341