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Handbook of Microbiological Quality Control Water-Insoluble Drug Formulation Second Edition Edited by
Pharmaceuticals and Medical Devices Edited by
Rosamund M. Baird University of Bath, UK
Norman A. Hodges
Rong Liu
AustarPharma, Edison, New Jersey, USA
Scientists have attributed more than 41% of the failures in new drug development to poor biopharmaceutical properties, particularly water insolubility The most comprehensive resource on the topic, this volume brings together a distinguished team of experts to provide step-by-step guidance on drug and water properties. Twenty-three chapters systematically describe solubility properties and their impact on formulation, from theory to industrial practice. With detailed discussion on how they contribute to solubilization and dissolution, the text also features three brand new chapters on water-insoluble drugs, exploring regulatory aspects, pharmacokinetic behaviors, and formulation strategies. Catalog no. 9644, ISBN: 978-0-8493-9644-1 2008, 7 x 10, 688 pp. Suggested Price: $299.95 / £167.00
Fate of Pharmaceuticals in the Environment and in Water Treatment Systems
University of Brighton, UK
Stephen P. Denyer Cardiff University, UK
This volume offers a wealth of microbiological information not only on the practical issues facing the company microbiologist today, but also on the underlying principles of microbiological quality assurance. Written by leading experts in the field, The Handbook of Microbiological Quality Control: Pharmaceuticals and Medical Devices is the essential reference source for the professional microbiologist. It provides guidance on safe microbiological practices, including laboratory design and sampling techniques, and considers in depth the design, storage, use, and quality control of microbiological culture. Catalog no. TF2047, ISBN: 978-0-7484-0614-2 2001, 7 x 10, 280 pp. Suggested Price: $179.95 / £97.00
Laboratory Quality Assurance Manual and Templates Edited by
Donnell R. Christian, Jr.
Professional Business Solutions, Chesterfield, Missouri, USA
Edited by
Stephanie Drilling
Diana S. Aga
Series: International Forensic Science and Investigation
Written by experts from academia, government, and industry, Fate of Pharmaceuticals in the Environment and in Water Treatment Systems provides a multi-disciplinary perspective on the issues, discussing topics ranging from field studies documenting the occurrence of pharmaceuticals in environmental compartments, to laboratory studies determining the degradation kinetics and formation of by-products during treatment. The text provides data to help scientists, regulators, and engineers understand the factors that affect the environmental fate of pharmaceuticals in soil and water, develop best management practices, and optimize treatment systems for removal of these compounds from the environment.
Written by experts with global experience in setting up laboratories, this work provides templates for the various policies, procedures, and forms contained in a quality assurance manual of a laboratory seeking accreditation. It includes a criteria file that cross-references individual document templates to the corresponding accreditation criterion associated with ISO 17025. Originally developed for use in forensic laboratories, this material meets the standards of ISO 17025 and therefore has international applications for all laboratories. The book includes an interactive CD-ROM that can be customized to suit the purpose of any laboratory seeking accreditation.
University at Buffalo, New York, USA
Catalog no. 52322, ISBN: 978-1-4200-5232-9 2008, 6 x 9, 408 pp. Suggested Price: $144.95 / £79.99
Catalog no. 73044, ISBN: 978-1-4200-7304-1 July 2009, 7 x 10, 512 pp. Suggested Price: $795.00 / £539.00
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