Since 2005, OCT’s team of over 200 professionals has conducted over 300 clinical trials in Eastern Europe
OCT is the leading contract research organization in Russia. We have conducted hundreds of clinical trials in Eastern Europe, in both CEE and the CIS. Our team of 200+ professionals provides a full range of high-quality CRO services for Phase I-IV and BE studies, with therapeutic expertise in oncology, infectious disease, and all major therapeutic indications.
As pharmaceutical and biotechnology companies have turned toward outsourcing models in clinical research, OCT has established itself as one of the top contract research organizations worldwide. With strong local expertise and focus on quality, OCT ensures seamless clinical trial conduct and drug registration, on time and within budget. Our experienced team delivers a full range of CRO services including medical writing, consultancy, project management/monitoring, data management/biostatistics and turnkey service for clinical development.
Our portfolio spans all major therapeutic areas, including oncology, infectious disease, gastroenterology, cardiology and more. View All Therapeutic Area Experience.
OCT is a team of over 200 clinical trial services professionals. Our clinical department consists of highly qualified specialists with medical, pharmaceutical and chemical backgrounds. OCT is managed by experienced clinical research experts who have contributed to the company’s development and growth since its beginning.
Support and communication
The OCT team is always easy to reach: we are an email or a phone call away and always respond within 24 hours. We provide consulting on clinical trial strategy and design, site management and patient engagement solutions, regulatory and logistics support and timely updates on clinical trial progress.
Global Standards Compliant Studies
OCT works in full compliance with international standards (ICH GCP) and FDA/EMA requirements. Since 2005, we have been guiding our sponsors through the intricacies of conducting clinical trials in Eastern Europe, both when dealing with the Ministry of Health of Russia and FDA or EMA. We have also developed our own set of SOPs, which are regularly updated by our Quality Assurance department.
Our goal is to provide sponsors with full transparency from the first inquiry to the final step of the study. Prior to the project’s start, we conduct a thorough analysis and weigh of all the potential risks that might arise during the study, and prepare a risk management plan. In case risks occur, all the parties concerned are immediately informed and actions are taken in accordance with the plan.
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