A comparative evaluation of Regulatory requirements for Registration of Dietary Supplements in Brazil, Russia, India, China and South Africa

Kinjal Gajjar, Zuki Patel, Vinit Movaliya, Niranajan Kanaki, Shrikalp Deshpande, Maitreyi Zaveri
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Abstract

Nutraceuticals are products that are rich in nutrients and provide health benefits, because of many factors like lifestyle changes and change in the dietary habits of people now a day, these products are widely used. Among all the other categories of Nutraceuticals Dietary supplement comprises huge part of Nutraceuticals. They are distinguishable from conventional food or drugs. They are intended to use to supplement the normal diet. The terms, nomenclature and definitions of the dietary supplements vary throughout the world. Different countries have their own regulation and legislative requirements. In regulated countries streamlined regulations are there, while well-structured and streamlined regulations for Nutraceuticals are lacking in other countries. In developing and emerging nations the regulation of dietary supplements are constantly evolving. It is necessary that the product complies all the regulatory requirements before they are placed on the market. The proposed study is based on the regulation and legislative requirements of dietary supplements in Brazil, Russia, India and South Africa.
对巴西、俄罗斯、印度、中国和南非膳食补充剂注册监管要求的比较评估
营养保健品是指富含营养成分并对健康有益的产品,由于生活方式的改变和人们日常饮食习惯的改变等诸多因素,这些产品被广泛使用。在所有其他种类的营养保健品中,膳食补充剂占营养保健品的很大一部分。它们与传统的食品或药物是有区别的。它们是用来补充正常饮食的。膳食补充剂的术语、命名法和定义在世界各地各不相同。不同的国家有自己的法规和立法要求。在受管制的国家,有简化的法规,而其他国家缺乏结构良好和简化的营养药品法规。在发展中国家和新兴国家,对膳食补充剂的监管不断发展。产品在投放市场之前必须符合所有的法规要求。这项拟议的研究是基于巴西、俄罗斯、印度和南非对膳食补充剂的监管和立法要求。
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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