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Více informací o knize International Regulatory Harmonization Amid Globalization of Drug Development

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Anotace knihy

The past several decades have been a time of rapid globalization in the development, manufacture, marketing, and distribution of medical products and technologies. Increasingly, research on the safety and effectiveness of new drugs is being conducted in countries with little experience in regulation of medical product development. Demand has been increasing for globally harmonized, science-based standards for the development and evaluation of the safety, quality, and efficacy of medical products. Consistency of such standards could improve the efficiency and clarity of the drug development and evaluation process and, ultimately, promote and enhance product quality and the public health. To explore the need and prospects for greater international regulatory harmonization for drug development, the IOM Forum on Drug Discovery, Development, and Translation hosted a workshop on February 13-14, 2013. Discussions at the workshop helped identify principles, potential approaches, and strategies to advance the development or evolution of more harmonized regulatory standards. This document summarizes the workshop.

Parametry knihy

Zařazení knihy Knihy v angličtině Medicine Medicine: general issues Medical equipment & techniques

• Plný název: International Regulatory Harmonization Amid Globalization of Drug Development
• Podnázev: Workshop Summary
• Autor: Forum on Drug Discovery, Development, and Transition, Board on Health Sciences Policy, Institute of Medicine
• Jazyk: Angličtina
• Vazba: Brožovaná
• Počet stran: 128
• EAN: 9780309284790
• ISBN: 0309284791
• ID: 04579517
• Nakladatelství: National Academies Press
• Rozměry: 229 × 152 mm
• Datum vydání: 24. November 2013

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