The production of pharmaceutical substances (API) is carried out on the basis of the License of the Ministry of Industry and Trade of Russia and its concordance with the Rules of Good Manufacturing Practice (GMP) is confirmed by the Conclusion.

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Pharmaceutical substances are registered by the Ministry of Health of Russia and the requirements to it are defined in the Pharmacopeia articles of the enterprise (FSP). Components for dietary supplements and food additives (dry and thick extracts) are produced in accordance with the Technical Conditions registered in Ros Accreditation, they have a Declaration of Conformity. Finished products intended for retail sale made on the basis of dry extracts were examined at the Institute of Nutrition of the Russian Academy of Medical Sciences and received Certificates of State Registration in Russian Federal Consumer Rights Protection and Human Health Control Service.