Documentation

Our Registration Department prepares all the necessary technical documentation to obtain the registration of each product for any country that you may need, we provide all required documentation and during the entire process. As a private label manufacturer, we will provide everything you need to sell your high quality product. 

Some of the necessary documents may include:

  1. Sale Certificate: declare quail-quantitative formulation, duly legalized.

  2. GMP or Good Manufacturing Practices: issued by the official sanitary authority, duly legalized in case of imported products.

  3. Dossier:

  • Proposed name.

  • Layout of text of packaging materials.

  • Quali-quantitative formulation, to corroborate and support the use of extra active ingredients added to the formula.

  • Monograph of the product.

  • Packaging material specifications.

  • Manufacturing: procedure description in detail, Master formula, Manufacturing Order (of an industrial batch, with corresponding signatures verifying the quantities weighed), in-process controls.

  • Analytical procedure for the active ingredients and the finished product: specifications, physicochemical characteristics, identification and assay of the active ingredient in the finished product. 

  • Type of package (bulk, for sale).

This is some of the necessary documentation for product registration and it will differ from country to country.

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