安全使用草药的历史 - 记录证据的方法

IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE

Journal of Ayurveda and Integrative Medicine Pub Date : 2024-01-01 DOI:10.1016/j.jaim.2023.100849

D.B. Anantha Narayana , N.B. Brindavanam , Sabina Shirsekar

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引用次数: 0

摘要

监管机构批准不同国家的草药贸易是一个漫长的过程，涉及提交不同类别草药的质量、安全和疗效数据。在过去十年中，提交草药使用历史记录的做法在全球范围内日益盛行。欧盟指令》和《印度食品条例》明确规定了这一要求。然而，作者还没有看到任何关于如何记录此类证据的广泛指南。本文试图为更广泛的磋商提供意见，以制定准则。

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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History of safe use of herbs - Approaches for documenting evidence

Approval by regulatory authorities for commerce of herbs to different nations is lengthy process involving quality, safety, and efficacy data submission for the herbs under different category. Submission of documented history of use of herbs in such steps has gained momentum in the last decade globally. EU Directives and Food Regulations, India, specifically describes this requirement. However, authors have not seen any broad guidelines on how to document such evidence. This paper attempts to provide inputs for wider consultations to lead to guideline development.

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来源期刊

Journal of Ayurveda and Integrative Medicine INTEGRATIVE & COMPLEMENTARY MEDICINE-

CiteScore

4.70

自引率

12.50%

发文量

136

审稿时长

30 weeks