Register pharmaceuticals and formulations in Russia as the reference state for the Eurasian Economic Union (EAEU). Conduct in-depth dossier review, modify as needed, and ensure alignment with all requirements.

Obtain registration certificates for medical devices according to national and EAEU regulations. Thoroughly evaluate registration dossiers and adjust documentation appropriately.

GMP Compliance Auditing Audit in accordance with Good Manufacturing Practice (GMP) standards approved by the Russian Ministry of Industry and Trade (Minpromtorg RF).

Execute pharmacovigilance functions for all registered medicinal products across EAEU member states.