Statandocs today is a multi-profile, dynamically developing company that offers a wide range services that are of high demand within the pharmaceutical industry. For clinical and observational studies (including RWE) we prepare complete essential documents package, support submission process, develop and maintain eCRF and IWRS, conduct validation and statistical analysis of data with preparation of interim and final study report. For registration dossiers (national, EAEU) we prepare all CTD modules, including CTD overview (module 2), assist in submissions, develop and conduct user testing for patient information leaflets, provide cloud service for eCTD XML EAEU for dossier preparation and life-cycle maintenance. We perform pharmacovigilance activities during clinical trials and after market authorization, including development of SOPs, master-file, RMP, conduct literature monitoring and prepare PSURs and DSURs. Statandocs offers various trainings and educational programs both in online format and as face-to-face sessions. Moreover, we actively work in the area of scientific medical writing, preparing materials for physicians and patients, articles (including systematic review and meta-analyses), posters and presentations. Our staff includes over 65 employees, including the highest medical writer head count in the region. We conducted over 1100 various projects for 94 clients in Russia, EAEU and CIS, including big international, regional and local pharmaceutic companies and CROs. Documents and services offered by us are well accepted by regulatory bodies in Armenia, Belarus, Vietnam, Georgia, Kazakhstan, Moldova, Russian Federation, Tadzhikistan, Uzbekistan, Ukraine, and USA. Statandocs is a reliable partner, we evolve rapidly, do not fear the most complex challenges and are at all times ready for productive cooperation.