About us

OCT is the leading CRO in Russia, with operations in CEE and the CIS region. With a team of 200 professionals, OCT provides a full range of high-quality research services for Phase I-IV and BE studies.


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 both standalone services such as medical writing, consultancy, project management/monitoring, data management/biostatistics and turnkey service for clinical development.


Since 2005, OCT has been working on 300 full-service and functional service projects in a number of therapeutic areas.

300

completed projects
since 2005 

14+

years of
experience

1,600+

research
centers

45,000+

enrolled
patients

Experienced team


OCT is a team of over 200 professionals. Our clinical department consists of highly qualified specialists with medical, pharmaceutical and chemical background. OCT is managed by experienced leaders who stood at the dawn of company's foundation and have been contributing to its development and growth ever since.
the day it was started.

Support and communication

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 the clinical trial strategy and design, regulatory and logistics support, timely updates on clinical trial progress.

Global Standards Compliant Studies

OCT works in full compliance with the international standards (ICH GCP) and FDA/EMA requirements. Since 2005, we
have been guiding our sponsors through
the intricacies of the regulatory system
both when dealing with the Ministry of Health of Russia and FDA or EMA. We are proud of our own set of SOPs developed and regularly updated by the Quality Assurance department.

Risk-management Approach

Our goal is to provide sponsors with full transparency from the first inquiry to the final step of the study. Prior to the project start, we conduct thorough analysis and weigh-in of all the potential risks and ambiguities that might arise during the study, and prepare risk-management plan. In case risks occur, all the parties concerned are immediately informed and actions are taken in accordance with the plan.

Our partners