Accelerating Clinical Research and Regulatory Solutions

Clinres Farmacija offers over 20 years of experience and expertise to accelerate clinical research, regulatory affairs, pharmacovigilance, and quality assurance for pharmaceutical and medical device development. With 200+ clinical trials conducted, 5000+ patients enrolled, and 550+ research sites, we provide comprehensive services for every stage of bringing new medicines and devices to market. Our full-service approach covers study design, trial operations, data management, regulatory submissions, post-marketing surveillance, and more. We partner with sponsors worldwide to navigate complex regulatory environments and ensure timely, compliant, and successful product approvals. With seasoned leadership and dedicated staff, Clinres delivers the experience, capabilities, and global footprint needed to achieve your development and commercialization goals.