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Controlled Release of Pesticides and Pharmaceuticals, D. H. Lewis


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Автор: D. H. Lewis
Название:  Controlled Release of Pesticides and Pharmaceuticals
ISBN: 9781475707397
Издательство: Springer
Классификация:

ISBN-10: 1475707398
Обложка/Формат: Paperback
Страницы: 340
Вес: 0.56 кг.
Дата издания: 30.04.2013
Язык: English
Размер: 244 x 170 x 19
Основная тема: Pharmacy
Ссылка на Издательство: Link
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Поставляется из: Германии


The Contribution of Acute Toxicity Testing to the Evaluation of Pharmaceuticals

Автор: Dietrich Schuppan; Anthony D. Dayan; Frances A. Ch
Название: The Contribution of Acute Toxicity Testing to the Evaluation of Pharmaceuticals
ISBN: 3642703925 ISBN-13(EAN): 9783642703928
Издательство: Springer
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Цена: 19591.00 р.
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Описание: International Symposium. IFPMA Symposium, Geneva 30-31 October 1984

Bioanalysis of Pharmaceuticals

Автор: Hansen Steen Honor
Название: Bioanalysis of Pharmaceuticals
ISBN: 1118716825 ISBN-13(EAN): 9781118716823
Издательство: Wiley
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Цена: 7437.00 р.
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Описание: Bioanalysis of Pharmaceuticals: Sample Preparation, Separation Techniques and Mass Spectrometry is the first student textbook on the separation science and mass spectrometry of pharmaceuticals present in biological fluids with an educational presentation of the principles, concepts and applications.

Human Pharmaceuticals in the Environment

Автор: Bryan W. Brooks; Duane B. Huggett
Название: Human Pharmaceuticals in the Environment
ISBN: 149390163X ISBN-13(EAN): 9781493901630
Издательство: Springer
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Цена: 16977.00 р.
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Описание: Human pharmaceuticals represent environmental contaminants of emerging concern. This book examines topics ranging from regulations and exposure analysis to comparative pharmacology and pharmaceutical take back programs.

Safety Evaluation of Biotechnologically-derived Pharmaceuticals

Автор: Susan A. Griffiths; C. Lumley
Название: Safety Evaluation of Biotechnologically-derived Pharmaceuticals
ISBN: 9401060436 ISBN-13(EAN): 9789401060431
Издательство: Springer
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Цена: 13974.00 р.
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Описание: Considerable investment has been made by both pharmaceutical and biotechnology companies in pharmaceutical products of biotechnology. However, because relatively few of these products have been marketed, lack of relevant experience means that uncertainty still surrounds the most appropriate strategy for their safety evaluation. The 13th CMR International Workshop, held in February 1997, provided the opportunity for regulatory authority and industry experts from Europe, Japan and the USA to share their experiences of designing safety evaluation programmes for specific product classes: colony stimulating factors, growth factors, hormones, interferons, interleukins, monoclonal antibodies for therapeutic use, and gene therapy products. Participants worked together to recommend those studies that should be considered for such safety evaluation, and those that may be unnecessary. These recommendations subsequently made a valuable contribution to the ICH guideline Safety Studies for Biotechnological Products', which was finalised at ICH 4 in Brussels in July 1997. The Workshop proceedings not only describe the recommendations but also provide the reader with an appreciation of the science behind safety evaluation strategies used by experts, the influence of different regulatory systems on these strategies, and the type of data required by both toxicologists and clinicians before they have sufficient confidence to administer pharmaceutical products of biotechnology to humans.

Methods for Stability Testing of Pharmaceuticals

Автор: Bajaj
Название: Methods for Stability Testing of Pharmaceuticals
ISBN: 1493976850 ISBN-13(EAN): 9781493976850
Издательство: Springer
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Цена: 11878.00 р.
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Описание: This detailed volume collects numerous methods and protocols related to different aspects of stability programs that are followed in pharmaceutical development laboratories. Implementation of a successful stability program, vital in preventing product failures and recalls, requires critical and logical thinking that goes beyond the regular documented protocols and methods, so the experiences of the book’s internationally-based expert contributors fill the chapters with practical guidance. As a volume in the Methods in Pharmacology and Toxicology series, this book presents the kind of real-world advice that is essential for advancing laboratory research. 


Authoritative and thorough, Methods for Stability Testing of Pharmaceuticals serves as a valuable addition to the existing armamentarium of resources available to stability testing personnel in research and industry.
Safety Evaluation of Pharmaceuticals and Medical Devices

Автор: Shayne C. Gad
Название: Safety Evaluation of Pharmaceuticals and Medical Devices
ISBN: 148998187X ISBN-13(EAN): 9781489981875
Издательство: Springer
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Цена: 19589.00 р.
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Описание: The inspiration for this text was the 1988 volume by Alder and Zbinden. Since then, much has changed. But the intent of this volume is to provide similar guidance as to what nonclinical safety assessment tests need to be performed to move a drug into man.

Raman and SERS Investigations of Pharmaceuticals

Автор: Monica Baia; Simion Astilean; Traian Iliescu
Название: Raman and SERS Investigations of Pharmaceuticals
ISBN: 364209693X ISBN-13(EAN): 9783642096938
Издательство: Springer
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Цена: 19589.00 р.
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Описание: Interdisciplinary research is the key to success in the sciences` future. This is the first book dealing with applications of the method SERS. It includes theory as well as experimental measurements.


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