Encyclopedia of Pharmaceutical Science and Technology, Fourth Edition, Six Volume Set (Print)

Encyclopedia of Pharmaceutical Science and Technology, Fourth Edition, Six Volume Set (Print) PDF

Author: James Swarbrick

Publisher: CRC Press

Published: 2013-07-01

Total Pages: 0

ISBN-13: 9781841848198

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Pharmaceutical science deals with the whole spectrum of drug development from start to finish. There are many different facets to the pharmaceutical industry, from initial research to the finished product, including the equipment used, trials performed, and regulations that must be followed. Presenting an overview of all of these different aspects, the Encyclopedia of Pharmaceutical Science and Technology, Fourth Edition is a must-have reference guide for all laboratories and libraries in the pharmaceutical field. Bringing together leaders from every specialty related to pharmaceutical science and technology, this is the single-source reference at the forefront of pharmaceutical R&D. The strength of this work is not only its breadth but also the caliber of contributing writers, all experts in their field, writing on all aspects of pharmaceutical science and technology. The fourth edition offers 29 new chapters ranging from biomarkers, computational chemistry, and contamination control to high-throughput screening, orally disintegrating tablets, and quality by design. The encyclopedia details best practices of equipment used, methods for manufacturing, options for packaging, and routes for drug delivery. The volumes also provide a thorough understanding of the choices behind each method. In addition, the regulations, safety aspects, patent guidance, and methods of analysis are presented. Key Areas Covered: Analytics Biomarkers Dosage forms Drug delivery Formulation Informatics Manufacturing Packaging Processing Regulatory affairs Systems validation This is an authoritative reference source for those practicing in any area of pharmaceutical science and technology, enabling the pharmaceutical specialist and novice alike to keep abreast of developments in this constantly evolving and highly competitive field. * Online version coming soon. Contact us to inquire about subscription options and print/online combination packages. US: (Tel) 1.888.318.2367 / (E-mail) [email protected] International: (Tel) +44 (0) 20 7017 6062 / (E-mail) [email protected]

Encyclopedia of Pharmaceutical Technology

Encyclopedia of Pharmaceutical Technology PDF

Author:

Publisher:

Published: 1988

Total Pages:

ISBN-13:

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Covers the discovery development,regulation, manufacturing, and commercialization of drugs and dosage forms. Includes pharmaceuticals,pharmacokinetics, analytical chemistry, quality assurance, toxicology and the manufacturing process.

Encyclopedia of Pharmaceutical Technology

Encyclopedia of Pharmaceutical Technology PDF

Author: James Swarbrick

Publisher: CRC Press

Published: 2013-07-01

Total Pages: 880

ISBN-13: 1439808236

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Presenting authoritative and engaging articles on all aspects of drug development, dosage, manufacturing, and regulation, this Third Edition enables the pharmaceutical specialist and novice alike to keep abreast of developments in this rapidly evolving and highly competitive field. A dependable reference tool and constant companion for years to com

Encyclopedia of Pharmaceutical Technology

Encyclopedia of Pharmaceutical Technology PDF

Author: James Swarbrick

Publisher: CRC Press

Published: 2000-12-05

Total Pages: 342

ISBN-13: 9780824728199

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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!

Encyclopedia of Pharmaceutical Technology, Third Edition (Print)

Encyclopedia of Pharmaceutical Technology, Third Edition (Print) PDF

Author: James Swarbrick

Publisher: CRC Press

Published: 2006-10-25

Total Pages: 5536

ISBN-13: 9780849393990

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Presenting authoritative and engaging articles on all aspects of drug development, dosage, manufacturing, and regulation, this Third Edition enables the pharmaceutical specialist and novice alike to keep abreast of developments in this rapidly evolving and highly competitive field. A dependable reference tool and constant companion for years to come, the Third Edition will offer completely new entries that cover critical issues in the field such as the impact of genomics, biotechnology, and implants on drug discovery, targeting, delivery, and formulation. In addition, it will address new regulatory issues, such as the changes in advertising regulations, and emerging FDA procedures.

Encyclopedia of Pharmaceutical Technology

Encyclopedia of Pharmaceutical Technology PDF

Author: James Swarbrick

Publisher: CRC Press

Published: 1995-03-23

Total Pages: 512

ISBN-13: 9780824728113

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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!

Pharmaceutical Manufacturing Encyclopedia

Pharmaceutical Manufacturing Encyclopedia PDF

Author: Marshall Sittig

Publisher:

Published: 1988

Total Pages: 938

ISBN-13:

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Organized by generic pharmaceutical, describes the manufacturing process. Data includes the therapeutic function, chemical and common names, raw materials contained, the CAS registry, numbers, plus a world-wide list of trade names and manufacturers.

Encyclopedia of Pharmaceutical Technology

Encyclopedia of Pharmaceutical Technology PDF

Author: James Swarbrick

Publisher: CRC Press

Published: 1988-10-13

Total Pages: 504

ISBN-13: 9780824728007

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"The Encyclopedia of Pharmaceutical Technology presents up-to-date and interdisciplinary contributions by leading international authorities in all areas of drugs and drug delivery systems. Major components of the Encyclopedia cover drugs, including physicochemical properties, preformulation, incompatibilities, metabolism, pharmacokinetics, stability, and decomposition...drug delivery systems (and devices), encompassing development, routes of administration, formulation alternatives, dosage form selection, scale up, manufacturing, process validation, bioavailability, and computerization...post-production considerations, ranging from patient compliance and physicians' preferences to national and international agencies; and more."