CROTURK - Full Service Turkish Contract Research Organization - CRO TURK

CROTURK is a full-service Turkish Contract Research Organization (CRO), strategically headquartered in Turkey, and founded with a vision to lead and facilitate high-quality, compliant, and efficient clinical research across the globe. With a solid foundation in regulatory expertise, operational excellence, and a deeply rooted understanding of the Turkish and broader EMEA (Europe, Middle East, Africa) clinical landscape, we are dedicated to advancing medical science and supporting the development of innovative therapies and devices through a full spectrum of clinical trial services. Established as a dynamic and versatile enterprise, CROTURK specializes in the comprehensive management of multinational clinical trials, with a commitment to delivering excellence across all phases of clinical development—from Phase I to Phase IV—as well as specialized medical device trials, including CE-mark and non-CE performance evaluations. At CROTURK, we offer a robust portfolio of services designed to support our clients through every stage of the clinical development lifecycle. Our end-to-end CRO capabilities ensure a seamless experience, driven by regulatory precision, operational agility, and scientific integrity. We navigate complex regulatory landscapes with ease. Our regulatory affairs team is adept at preparing and submitting applications, securing approvals, and maintaining compliance throughout the study lifecycle. With deep expertise in Turkish Ministry of Health (MoH) regulations and international standards (EMA, FDA, ISO), we provide our clients with accurate, efficient, and strategic guidance. Our GCP-trained monitors ensure high-quality site management and data integrity through proactive site engagement, rigorous adherence to protocols, and prompt issue resolution. Our monitoring services extend across all phases of pharmaceutical and device studies, with tailored oversight for each project’s unique needs.