Certificate of Registration will be made out in the Department and for each item separately.

The cost of certificate on a name-

*The cost depends on the source of some components will be every BAA(Biologically active additive)and the amount of these components.These components will undergo quantitative and qualitative identification,and so varies the price.

Registration deadline-about 1.5-2 month.

Required documents:

1.Power of Attorney(sample available)

2.A certificate issued by a third party,certifying the safety of products(certificates of free sale,certificate of health)

3.Ingredient composition with the percentage of components and/or formulation

4.The specification for the product(information on packaging of dietary supplements+description)

5.Test protocols from the manufacturer(if available)

6.Original Label

7.Technological scheme of production-if

8.Certificate of Conformity/Declaration of GMP standard production and/or ISO and/or HACCP-the presence of

9.Samples(200 g/of 4.Per item)

10.The declaration of the manufacturer in the absence of PD pesticides,hormones,psychotropic drugs and potent substances and ingredients derived from GMOs and the use of nanotechnology-can prepare themselves

11.copy extracts from the Unified State Register of legal entities of the firm by proxy+stamped sheets or

12.Invoice(any transport document)for the samples with a mark of customs that allowed importation

营养品或保健品注册要求资料（BAA）Certificate of Registration will be made out in the Department and for each item separately

登记证书将在该部制作，每个项目分开做

一个名称的证书成本——从37880美金开始。

成本取决于一些组件的来源，每个BAA（生物活性添加剂）和这些组件的数量。这些组件将进行定量和定性鉴别，因此价格会有所不同。

登记最终时间——约1.5-2个月。

需要的文件：

1、委托书（样本可提供）

2、由第三方颁发的证书，证明产品的安全性（自由销售证书，健康证书）

3、组件的百分比和/或制定的成分组成

4、产品规格（膳食补充剂的包装上的信息+描述）

5、制造商测试协议（如果有）

6、原产地标签

7、生产技术方案-如果

8、合格证书/GMP标准生产和/或国际标准化组织（ISO）和/或HACCP——存在-

9、样品（4/200克，每件）

10、制造商出具的，申明无PD农药，激素，精神药品、振奋剂，使用转基因生物和纳米技术——可以自己编写

11、联邦注册实体公司代理副本+加盖表格

12、带有表明海关允许进口标志的样品发票（任何运输文件）

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