印尼中药品牌的监督与注册

Tjia Siauw Jan, Tri Handayani, Memed Sueb
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引用次数: 1

摘要

传统药物(草药、标准化草药、植药(临床草药)、进口传统药物)是以植物成分、动物成分、矿物成分、galenic制剂或这些成分的混合物形式存在的一种或多种草药成分,世世代代用于治疗,并可按社会通行的规范使用。本研究旨在了解和分析印尼传统医药品牌监管注册的相关情况。本研究采用定性方法和规范的司法方法。数据收集技术是通过图书馆研究进行的。可以得出结论,中药品牌注册的监管必须由国家药品和食品管理局(NADFC)最大限度地进行。这避免了在监视过程不透明的情况下出现的问题。良好和适当的监督必须以法治为基础,因为印度尼西亚承认法律的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Supervision and Registration of Traditional Medicine Brand in Indonesia
Traditional medicine (herbal medicine, standardized herbal medicine, phytopharmaca (clinical-based herbal medicine), imported traditional medicine) is an ingredient or herb ingredients in the form of plant ingredients, animal ingredients, mineral ingredients, galenic preparations, or a mixture of such ingredients that have been used for treatment for generations, and can be applied by the norms prevailing in the society. This study aims to find out and analyze related to the supervision and registration of traditional medicine brands in Indonesia. This research uses a qualitative method with a normative juridical approach. Data collection techniques are carried out through library studies. It can be concluded that the supervision of traditional medicine brands' registration must be carried out to the maximum by the National Agency of Drug and Food Control (NADFC). This avoids the problems that will arise in the event of the obscurity of the surveillance process. Good and proper supervision must be based on the rule of law because Indonesia recognizes the Law's existe.
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