The Assessment of The Quality, Efficacy and Safety of The Investigational Medicinal Product in The Absence of An Approved Registration Dossier

V. Ekaterina
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Abstract

Today the pharmaceutical industry is one of the highly regulated fields with many rules and regulations which are quite volatile and are updated at least every decade [1-8]. Practical guidelines and recommendations are published by regulatory authorities and manufacturers even more often. As a result, things that were state-of-the art yesterday may not be appropriate tomorrow, especially in the rapidly changing area of biopharmaceutical development.
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在没有批准注册档案的情况下,临床试验药品的质量、疗效和安全性评估
今天,制药行业是高度管制的领域之一,有许多规则和条例,这些规则和条例相当不稳定,至少每十年更新一次[1-8]。监管机构和制造商甚至更频繁地发布实用指南和建议。因此,昨天最先进的东西明天可能就不合适了,特别是在快速变化的生物制药开发领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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