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FDA 有关文件的诠释 By Dr. OlympiaLiu
(12/22/2014)
According to the FDA document:
In June, 2007, FDA published
comprehensive regulations for Current Good Manufacturing Practices for those
who manufacture, package or hold dietary supplement products. These regulations
focus on practices that ensure the identity, purity, quality, strength and
composition of dietary supplements.
如果您懂英语,您该明白,此是专指“Manufacturing Practices”,即对大批生产者的管理。
那是针对近年来,一振风刮起的工厂大批生产中药而制定的管理文件。
而Dr. Liu’s vegetable Herb,it’s food, 是保健食品, yard sell price. Plus, total just 2 lbs. in the yr of 2014.
Dr, Liu’s Vegetable Herb which is a kind of herb in the Grocery Store, is Bulk Herb.
It total different from “Manufacturing Practices”! 您的帽子店生意不好,也甭给人廉带!!
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By the way, 每月我收FDA, CDC,WHO , as well as NHI,… 他们从Gov。 直接寄给我文件。
定期 给我Update Document。但,由于忙,有的就堆到那里,没空儿看。
作为168 “针灸中医”的版主,今后,我会定期向网友翻译并发布Gov。有关医疗健康及保险的重要文件。 请关注。 |
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