6. Entering pharmaceutical substance in the State Register of Medical Remedies

7. Confirmation of the state registration of medicinal product

8. Organization and follow up of preclinical trials of medicinal product

9. Organization and follow up of clinical trials of medicinal product

10. Registration/re-registration of selling price limit for medicinal product

11. Initial evaluation of registration dossier

12. Provision of information about registered medicinal products and pharmaceutical substances, about any analogues in the market or lack thereof