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

V. Ekaterina
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引用次数: 0

摘要

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