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Safety Evaluation of Pharmaceuticals and Medical Devices, Shayne C. Gad


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Автор: Shayne C. Gad
Название:  Safety Evaluation of Pharmaceuticals and Medical Devices
ISBN: 9781489981875
Издательство: Springer
Классификация:



ISBN-10: 148998187X
Обложка/Формат: Paperback
Страницы: 126
Вес: 0.20 кг.
Дата издания: 08.10.2014
Язык: English
Размер: 234 x 156 x 8
Основная тема: Biomedicine
Подзаголовок: International Regulatory Guidelines
Ссылка на Издательство: Link
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Поставляется из: Германии
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.


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

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.


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