All documents necessary for the medicinal product’s submission must conform to the local or EAEU region requirements. The unified information system in the Eurasian Economic Union region has its specific requirements for local regulatory document preparations.

Biomapas services include the preparation of Normative Documents (ND) in accordance with EAEU regulations and Ph standards for the quality control of a medicinal product. A translation of the documents can be provided if needed.

For any inquiry regarding our services, please contact Biomapas Business Development team.

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