Encyclopedia of Pharmaceutical Technology
Volume 13 - Preservation of Pharmaceutical Products to Salt Forms of Drugs and Absorption
1st Edition
Published on 24. October 1995
Book
Hardback
552 pages
978-0-8247-2812-0 (ISBN)
Description
The Encyclopedia of Pharmaceutical Technology presents authoritative and contemporary articles on all aspects of drug development, dosage forms, manufacturing, and regulation-enabling the specialist and novice alike to keep abreast of developments in this rapidly evolving and highly competitive field.
A dependable reference tool and a solid investment for years to come--maintaining currency through its supplements [Volume 18/Supplement 1: Published November, 1998]
The Encyclopedia contains interdisciplinary contributions in a wide array of subjects, including
Drugs
decomposition
metabolism
pharmaceutical incompatibilities
pharmacokinetics
physicochemical properties
preformulation
stability
Drug Delivery Systems and Devices-Development and Manufacture
analysis and controls
bioavailability
use of computerization
formulation and processing alternatives
national and international registration
packaging
patents
process validation
scale-up
safety and efficacy
stability
standards
Post-Production and Practical Considerations
governmental/industrial/professional organizations
legal aspects
national and international agencies
patent life of drugs
patient compliance
...and much, much more!
A dependable reference tool and a solid investment for years to come--maintaining currency through its supplements [Volume 18/Supplement 1: Published November, 1998]
The Encyclopedia contains interdisciplinary contributions in a wide array of subjects, including
Drugs
decomposition
metabolism
pharmaceutical incompatibilities
pharmacokinetics
physicochemical properties
preformulation
stability
Drug Delivery Systems and Devices-Development and Manufacture
analysis and controls
bioavailability
use of computerization
formulation and processing alternatives
national and international registration
packaging
patents
process validation
scale-up
safety and efficacy
stability
standards
Post-Production and Practical Considerations
governmental/industrial/professional organizations
legal aspects
national and international agencies
patent life of drugs
patient compliance
...and much, much more!
More details
Series
Language
English
Place of publication
New York
United States
Publishing group
Taylor & Francis Inc
Target group
College/higher education
Professional and scholarly
Dimensions
Height: 279 mm
Width: 216 mm
Weight
1406 gr
ISBN-13
978-0-8247-2812-0 (9780824728120)
Copyright in bibliographic data is held by Nielsen Book Services Limited or its licensors: all rights reserved.
Schweitzer Classification
Persons
Content
Preservation of Pharmaceutical Products, Sally F. Bloomfield and Fiona C. Sheppard
Preservative Testing, Norman A. Hodges and Stephen P. Denyer
Prodrugs, Lona L. Christrup, Judi Moss, and Bente Steffansen
Product License Applications (PLAs) and Establishment License Applications (ELAs) for Biological Products, Dhiren N. Shah and James G. Kenimer
Project Management, Jerome J. Groen
Protein Binding of Drugs, Sylvie Laganie and Iain J. McGilveray
Pyrogens and Pyrogen Testing, Marlys E. Weary
Quality Assurance of Drug Products, Richard Kaplan
Radiation Sterilization of Drugs, Stephen G. Schulman and Phillip M. Achey
Radiochemical Methods of Analysis, Kumaril Bhargave, Jie Du, Rajagopalan Raghavan, and Jose Joseph
Receptors for Drugs, Jeffrey M. Herz, William J. Thomsen, Richard Mitchell, and George G. Yarbrough
Rectal Administration and Absorption of Drugs, Joseph A. Fix and J. Howard Rytting
Registration of Drugs, William J. C. Currie and Richard W. J. Currie
Rheology of Pharmaceutical Systems, Brian Warburton
Robotics in the Pharmaceutical and Biomedical Laboratory, J. Wieling
Salt Forms of Drugs and Absorption, Lyle D. Bighley, Stephen M. Berge, and Donald C. Monkhouse
Index to Volume 13
Preservative Testing, Norman A. Hodges and Stephen P. Denyer
Prodrugs, Lona L. Christrup, Judi Moss, and Bente Steffansen
Product License Applications (PLAs) and Establishment License Applications (ELAs) for Biological Products, Dhiren N. Shah and James G. Kenimer
Project Management, Jerome J. Groen
Protein Binding of Drugs, Sylvie Laganie and Iain J. McGilveray
Pyrogens and Pyrogen Testing, Marlys E. Weary
Quality Assurance of Drug Products, Richard Kaplan
Radiation Sterilization of Drugs, Stephen G. Schulman and Phillip M. Achey
Radiochemical Methods of Analysis, Kumaril Bhargave, Jie Du, Rajagopalan Raghavan, and Jose Joseph
Receptors for Drugs, Jeffrey M. Herz, William J. Thomsen, Richard Mitchell, and George G. Yarbrough
Rectal Administration and Absorption of Drugs, Joseph A. Fix and J. Howard Rytting
Registration of Drugs, William J. C. Currie and Richard W. J. Currie
Rheology of Pharmaceutical Systems, Brian Warburton
Robotics in the Pharmaceutical and Biomedical Laboratory, J. Wieling
Salt Forms of Drugs and Absorption, Lyle D. Bighley, Stephen M. Berge, and Donald C. Monkhouse
Index to Volume 13