In the world of clinical research and medicine, where every detail matters, high-quality study design and regulatory-compliant documentation play a crucial role. The team of professionals at OCT possesses deep knowledge and experience, ready to take on the development of drug registration strategies, clinical trial designs, and a full spectrum of documentation that meet the most stringent requirements of local and international regulatory bodies, as well as publishing standards. In addition, our experts are active members of the European Medical Writers Association (EMWA), which guarantees their high qualifications and continuous development in the industry. Beyond a deep understanding of regulatory requirements, our experts possesses extensive experience in various therapeutic areas and phases of clinical research, as well as a comprehensive knowledge of the nuances of clinical and statistical issues and processes.
OCT’s professionals provide scientific consulting and medical writing services both within turnkey projects and as separate services.
