You are currently browsing 1–10 of 294 new and published books in the subject of Pharmaceutical Science — sorted by publish date from newer books to older books.
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Series: Array
Knowledge of pharmacokinetics is critical to understanding the absorption, distribution, metabolism, and excretion of drugs. It is therefore vital to those engaged in the discovery, development, and preclinical and clinical evaluation of drugs, as well as practitioners involved in the clinical use...
Published February 8th 2012 by CRC Press
Series: Chapman & Hall/CRC Biostatistics Series
Nonpharmacological treatments include a wide variety of treatments such as surgery, technical procedures, implantable and non-implantable devices, rehabilitation, psychotherapy, and behavioral interventions. Unlike pharmacological treatments, these have no specific requirements for approval....
Published December 18th 2011 by Chapman & Hall
Because of many misconceptions, the biological drug manufacturing industry does not fully utilize disposable components, despite their wide availability. These misconceptions include concerns for the quality of materials, running costs, scalability, the level of automation possible, and the...
Published December 18th 2011 by CRC Press
Fermentation Microbiology and Biotechnology, Third Edition explores and illustrates the diverse array of metabolic pathways employed for the production of primary and secondary metabolites as well as biopharmaceuticals. This updated and expanded edition addresses the whole spectrum of fermentation...
Published December 11th 2011 by CRC Press
Series: Biotechnology and Bioprocessing
As with all of pharmaceutical production, the regulatory environment for the production of therapeutics has been changing as a direct result of the US FDA-initiated Quality by Design (QbD) guidelines and corresponding activities of the International Committee for Harmonization (ICH). Given the...
Published December 6th 2011 by CRC Press
Series: Chapman & Hall/CRC Biostatistics Series
With new statistical and scientific issues arising in adaptive clinical trial design, including the U.S. FDA’s recent draft guidance, a new edition of one of the first books on the topic is needed. Adaptive Design Methods in Clinical Trials, Second Edition reflects recent developments and...
Published November 30th 2011 by Chapman & Hall
The management of clinical data, from its collection during a trial to its extraction for analysis, has become a critical element in the steps to prepare a regulatory submission and to obtain approval to market a treatment. Groundbreaking on its initial publication nearly fourteen years ago, and...
Published October 25th 2011 by CRC Press
Series: Pharmacy Education Series
Completely revised and updated, this second edition of Pharmaceutical Dosage Forms and Drug Delivery elucidates the basic principles of pharmaceutics, dosage form design, and drug delivery. The authors integrate aspects of physical pharmacy, biopharmaceuticals, drug delivery, and biotechnology. The...
Published October 24th 2011 by CRC Press
Although complex and lengthy, the process of certification for the ISO 13485 can be easily mastered using the simple method outlined in ISO 13485: A Complete Guide to Quality Management in the Medical Device Industry. Written by an experienced industry professional, this practical book provides a...
Published October 19th 2011 by CRC Press
The focus of Biotechnology Fundamentals is to educate readers on both classical and modern aspects of biotechnology and to expose them to a range of topics, from basic information to complex technicalities. Other books cover subjects individually, but this text offers a rare topical combination of...
Published September 19th 2011 by CRC Press
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