000 | 03402nam a22004334a 4500 | ||
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001 | EBC427896 | ||
003 | MiAaPQ | ||
005 | 20240120130924.0 | ||
006 | m o d | | ||
007 | cr cn||||||||| | ||
008 | 080303s2009 njua sb 001 0 eng | ||
010 | _z 2008009573 | ||
016 | 7 |
_z101467523 _2DNLM |
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020 | _z9780470056097 (cloth) | ||
020 | _z0470056096 (cloth) | ||
035 | _a(MiAaPQ)EBC427896 | ||
035 | _a(Au-PeEL)EBL427896 | ||
035 | _a(CaPaEBR)ebr10296483 | ||
035 | _a(CaONFJC)MIL203105 | ||
035 | _a(OCoLC)437111461 | ||
040 |
_aMiAaPQ _cMiAaPQ _dMiAaPQ |
||
050 | 4 |
_aRM301.8 _b.F67 2009 |
|
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. Ann Arbor, MI : ProQuest, 2015. Available via World Wide Web. Access may be limited to ProQuest affiliated libraries. | ||
650 | 0 |
_aDrugs _xDose-response relationship. |
|
650 | 0 |
_aDrugs _xDosage. |
|
650 | 0 | _aOral medication. | |
650 | 0 | _aDrug development. | |
655 | 4 | _aElectronic books. | |
700 | 1 | _aZheng, Jack. | |
710 | 2 | _aProQuest (Firm) | |
856 | 4 | 0 |
_uhttps://ebookcentral.proquest.com/lib/bacm-ebooks/detail.action?docID=427896 _zClick to View |
999 |
_c40541 _d40541 |