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Church Fonts (Shire Library) Church Fonts (Shire Library) Национальная и зарубежная кухня Национальная и зарубежная кухня Greekish: Everyday recipes with Greek roots Greekish: Everyday recipes with Greek roots Australia's Lost Heroes: Anzacs in the Russian Civil War 1919 Australia's Lost Heroes: Anzacs in the Russian Civil War 1919 JavaScript by Doing: Over 100 Hands-On Coding Challenges for Mastering JS JavaScript by Doing: Over 100 Hands-On Coding Challenges for Mastering JS Advanced Machine Learning with Evolutionary and Metaheuristic Techniques Advanced Machine Learning with Evolutionary and Metaheuristic Techniques Природа человека и смысл истории Природа человека и смысл истории Иеротопия: создание сакральных пространств в Византии и Древней Руси Иеротопия: создание сакральных пространств в Византии и Древней Руси Горячая работа на холодной войне Горячая работа на холодной войне Python Programming Bible for Beginners: [4 in 1] The Ultimate 5-Day Python Crash Course with Step-by-Step Guidance Python Programming Bible for Beginners: [4 in 1] The Ultimate 5-Day Python Crash Course with Step-by-Step Guidance Кухня НКВД Кухня НКВД The Data Preparation Journey: Finding Your Way with R The Data Preparation Journey: Finding Your Way with R Русские плюс... Русские плюс... Тигров племянник Тигров племянник Complete History of the Universe Complete History of the Universe Есть ли вода в Море Дождей Есть ли вода в Море Дождей
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New Drug Approval Process: Accelerating Global Registrations, 4th Edition
Добавил: daromir / 28-12-2016, 19:45 /

Автор: Richard A. Guarino
Название: New Drug Approval Process: Accelerating Global Registrations, 4th Edition
Издательство: CRC Press
Год: 2004
ISBN: 978-0824750411
Серия: Drugs and the Pharmaceutical Sciences (Book 139)
Язык: English
Формат: pdf
Размер: 12,1 mb
Страниц: 668

Offering expert guidance on the clinical, regulatory, and statistical processes involved in the development of new pharmaceutical product applications for drugs, biologicals, and medical devices, the Fourth Edition details the specific regulations, guidelines, and procedures that will advance and ensure approval of United States and global new product applications. It communicates and integrates a new approach to the world of pharmaceutical personnel on all aspects of new product development and alerts readers to clinical and regulatory tasks that require immediate attention and long-term follow-up in order to comply with the international acceptance of new product approvals.







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