Using the biologic license application or new drug application as a basis for the common technical document.

MaryAnn Foote
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引用次数: 1

Abstract

With the introduction of the common technical document (CTD), many writers in the biotech and pharmaceutical industries are now required to submit dossiers in this format. The format of the CTD is not extremely difficult from the familiar documents of the Biologic License Application (BLA) or New Drug Application (NDA). The CTD can be mapped to existing areas of the BLA or NDA. The components of the CTD are discussed and references to the current guidance worldwide are provided to assist the writer.

以生物制品许可申请或新药申请作为通用技术文件的基础。
随着通用技术文件(CTD)的引入,生物技术和制药行业的许多作者现在被要求以这种格式提交档案。CTD的格式与我们所熟悉的生物制剂许可申请(BLA)或新药申请(NDA)的文件相比并没有太大的难度。CTD可被映射到陆地保护区或国家发展区的现有区域。讨论了CTD的组成部分,并提供了对世界范围内现行指南的参考,以协助作者。
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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