We provide drug registration in Russia, conduct bioequivalence studies, biosimilars, vaccines and orphan drugs registration, deliver regulatory consulting, manage clinical trials (phase I, phase II, phase III) and preclinical studies in Russia. We have over 15 years of extensive experience with Russian Healthcare system. Combining best planning and regulatory tactics we are confident to make your project done perfectly and on time. Our code of communication with health authorities is based on high ethical standards. 100% of our experts and managers have medical or pharmaceutical schools diplomas – majority of our experts have Ph.D. degrees. Our team is adherent to anticorruption legislation and measures. And we guarantee you quality at every stage of our work.