CATO SMS is a team that will tackle your toughest challenges with confidence and precision. With more than 30 years of global experience in drug development, our team is optimized for small and emerging biopharma sponsors like you. With offices across North America, Europe, and the Middle East, CATO SMS has experience conducting trials in more than 25 countries.
Our specialists deliver innovative regulatory consulting solutions to guide you through the most complex regulatory challenges. Our expert teams effectively design and execute clinical trials — from strategy to approval — in complex indications and modalities across a variety of therapeutic areas, with a proven center of excellence in oncology.
Our combination of regulatory, therapeutic, and operational expertise enables us to meet your challenges and seize opportunities that arise before or during study conduct. Whether you need experts in medical affairs, regulatory consulting services, or clinical trial management, we can help you meet your goals.