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Canadian Natural Health Products Regulations

机译:加拿大天然健康产品规定

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Canada's Regulations for natural health products were developed following extensive consultation with all stakeholder groups. They cover a wide variety of non-prescription materials including plants, their extracts and isolates, vitamins, minerals, amino acids, synthetic duplicates, probiotics, and homeopathic medicines. The Natural Health Products Regulations include provisions on definitions, product licensing, site licensing, good manufacturing practices, clinical trials, labelling and packaging requirements, and adverse reaction reporting. The Regulations will come into force on January 1, 2004 followed by a transitional period that will span from 2 to 6 years - 2 years for site licensing and 6 years for products with Drug Identification Numbers (DIN).
机译:加拿大加拿大自然健康产品的法规是通过与所有利益相关方团体进行广泛磋商而制定的。它们涵盖了各种非处方材料,包括植物,其提取物和分离物,维生素,矿物质,氨基酸,合成重复剂,益生菌和顺势疗法药物。天然保健品规定包括关于定义,产品许可,现场许可,良好制造实践,临床试验,标签和包装要求的规定,以及不良反应报告。该法规将于2004年1月1日生效,然后在2至6年 - 2年间为现场许可的过渡期,并为具有药物识别号码的产品(DIN)的产品6年。

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