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ELB178483 |
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FINmELB |
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20200520144314.0 |
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m o d | |
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cr cn||||||||| |
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080303s2009 njua sb 001 0 eng |
| 016 |
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|z 101467523
|2 DNLM
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| 020 |
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|z 9780470056097 (cloth)
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| 020 |
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|z 0470056096 (cloth)
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| 035 |
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|a (OCoLC)213008102
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|a FINmELB
|c FINmELB
|d FINmELB
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| 050 |
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|a RM301.8
|b .F67 2009
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|a 615/.1
|2 22
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| 245 |
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|a Formulation and analytical development for low-dose oral drug products
|h [electronic resource] /
|c edited by Jack Zheng.
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| 260 |
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|a Hoboken, N.J. :
|b John Wiley & Sons,
|c c2009.
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| 300 |
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|a xxiii, 461 p. :
|b ill.
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| 504 |
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|a Includes bibliographical references and index.
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| 505 |
0 |
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|a An 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 --
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| 505 |
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|a Analytical 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.
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| 588 |
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|a Description based on metadata supplied by the publisher and other sources.
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| 590 |
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|a Electronic reproduction. Santa Fe, Arg.: elibro, 2021. Available via World Wide Web. Access may be limited to eLibro affiliated libraries.
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| 650 |
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0 |
|a Drugs
|x Dose-response relationship.
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| 650 |
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0 |
|a Drugs
|x Dosage.
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| 650 |
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0 |
|a Oral medication.
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| 650 |
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0 |
|a Drug development.
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| 655 |
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4 |
|a Electronic books.
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| 700 |
1 |
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|a Zheng, Jack.
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| 797 |
2 |
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|a elibro, Corp.
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| 856 |
4 |
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|u https://elibro.uam.elogim.com/ereader/bidiuam/178483
|z Texto completo
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| 950 |
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|a eLibro English
|
