Formulation and analytical development for low-dose oral drug products

Guardado en:
Detalles Bibliográficos
Otros Autores: Zheng, Jack
Formato: Electrónico Libro electrónico
Lenguaje:Inglés
Publicado: Hoboken, N.J. : John Wiley & Sons, c2009.
Materias:
Drugs > Dose-response relationship.
Drugs > Dosage.
Oral medication.
Drug development.
Electronic books.
Acceso en línea:https://elibro.net/ereader/ufasta/178483
Aporte de:Registro referencial: Solicitar el recurso aquí
Biblioteca Universitaria H. Wast (UFASTA) de Universidad FASTA
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245 0 0 |a Formulation and analytical development for low-dose oral drug products  |h [electronic resource] /  |c edited by Jack Zheng. 
260 |a Hoboken, N.J. :  |b John Wiley & Sons,  |c c2009. 
300 |a xxiii, 461 p. :  |b ill. 
504 |a Includes bibliographical references and index. 
505 0 |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 -- 
505 0 |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. 
588 |a Description based on metadata supplied by the publisher and other sources. 
590 |a Electronic reproduction. Santa Fe, Arg.: elibro, 2021. Available via World Wide Web. Access may be limited to eLibro affiliated libraries. 
650 0 |a Drugs  |x Dose-response relationship. 
650 0 |a Drugs  |x Dosage. 
650 0 |a Oral medication. 
650 0 |a Drug development. 
655 4 |a Electronic books. 
700 1 |a Zheng, Jack. 
797 2 |a elibro, Corp. 
856 4 0 |u https://elibro.net/ereader/ufasta/178483 
950 |a eLibro English 
999 |c 206417  |d 206417 

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