Encyclopedia of Pharmaceutical Science and Technology, (6 volumes set) - 4th Ed (4th Ed.)
Coordonnateur : Swarbrick James
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.
Also Available Online
This Taylor & Francis encyclopedia is also available through online subscription, offering a variety of extra benefits for researchers, students, and librarians, including:
- Citation tracking and alerts
- Active reference linking
- Saved searches and marked lists
- HTML and PDF format options
Contact Taylor and Francis for more information or to inquire about subscription options and print/online combination packages.
US: (Tel) 1.888.318.2367; (E-mail) e-reference@taylorandfrancis.com
International: (Tel) +44 (0) 20 7017 6062; (E-mail) online.sales@tandf.co.uk
29 New Chapter Topics:
Automated Dissolution Testing
Biomarkers in Drug Discovery and Development
Computational Chemistry
Contamination Control: Cleanrooms and Clean Air Devices
Control of genotoxic impurities in pharmaceutical products
Crystal Form Analysis of Active Pharmaceutical Ingredients (APIs)
Drug Delivery using Electrophoresis
Drug Delivery: Inner Ear
Drug Transporters in ADME
Evolutionary Computing and Formulation Optimization
Freeze Drying of Biologicals
Good Publication Practice
High-Throughput Screening (HTS) in Drug Discovery
Impurity Identification in Pharmaceuticals
Injection Molding and its Drug Delivery Applications
Microcalorimetry in Pharmaceutical Development
Multivariate Statistical Analysis
Nano-Needle Systems for Vaccine Delivery
Oral Lipid-Based Formulations
Orally Disintegrating Tablets
Parenteral Formulation: Local Injection Site Reaction and Muscle Tolerance
Particle Shape Analysis
Proteins and Peptides: Physical and Chemical Stability
Quality by Design (QbD) and Analytical Method Development
Quality Target Product Profile (QTPP) for Pharmaceutical Packaging and Delivery Systems
Quality by Design (QbD) in Freeze Drying
Scale-Up of Solid Dispersions
Single-Use Processing in the Pharmaceutical Industry
Statistical Outliers: Methods and Applications
James Swarbrick, D.Sc., Ph.D., is the president of PharmaceuTech, Inc., Pinehurst, North Carolina, USA. He has served in a number of industrial and academic positions, including director of product development at Sterling-Winthrop Research Institute, Rensselaer, New York, and vice president for research and development and vice president for scientific affairs at AAIPharma, Wilmington, North Carolina, USA. Prior to joining AAIPharma, he was a professor and chairman of the Division of Pharmaceutics at the University of North Carolina at Chapel Hill School of Pharmacy.
Dr. Swarbrick is a Fellow of the American Association of Pharmaceutical Sciences, the Royal Society of Chemistry, and the Royal Pharmaceutical Society of Great Britain. He has also served as a member and chairman of the FDA’s Generic Drugs Advisory Committee, as chairman of the PhRMA Foundation’s Pharmaceutics Advisory Committee, as well as a member of the PhRMA Foundation’s Scientific Advisory Committee.
Date de parution : 07-2013
Ouvrage de 4296 p.
21x28 cm
Disponible chez l'éditeur (délai d'approvisionnement : 15 jours).
Prix indicatif 3444,66 €
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Mots-clés :
Biomarker, Dosage, Dosage form, Drug, Drug delivery, Manufacture, Pharmaceutical, Pharmacology, Pharmacy, Technology