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WELCOME TO CLINARTIS

Clinartis is a dynamic contract research organization serving pharmaceutical, biotech and medical device companies to support Phase I - IV drug and device development in US and Eastern Europe, including Russia, Ukraine, Serbia, Baltic countries and others. We provide a broad range of services to meet specific requirements of clinical research development programs according to the standards of Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.

Our broad therapeutic experience, strong project management capabilities, and core expertise in quality assurance and regulatory affairs enables us to address specific product development needs and mitigate obstacles often present in pharmaceutical and medical device development.  Clinartis is positioned to handle the most complex projects in variety of therapeutic areas covering the entire process of clinical development from study design through clinical study conduct and ultimately to regulatory submission. Organized by a group of clinical research, regulatory and quality professionals with diverse areas of expertise and experience, we offer a substantial global reach for clinical development programs, meeting the highest quality standards, and with utmost dedication to client satisfaction.

Clinartis is uniquely positioned to assist with your drug development programs. Our team of internal experts in collaboration with our network of physicians, regulatory professionals and scientists will help to move your novel scientific discoveries and innovative ideas to the market.