Medical writing is an important part of the clinical drug trials in Russia. Medical documents include the study essential documents, such as Investigator’s Brochure (IB), Study Protocol, Case Report Form (CRF), Informed Consent Form (ICF), Clinical Study Report (CSR), Clinical Study Report, Pre-clinical Report. All documents are prepared by the specialists with a great experience in drug trials.
OCT medical writers are members of the American and/or European Medical Writers Associations. They have participated in more than 200 drug clinical trials in Russia and Eastern Europe. Our team is also successfully involved in translating the medical documents for clinical trials of drugs in different therapeutic areas. If you need medical writing services in CIS, OCT will provide you with any document within tight deadlines.
Our colleagues in Ukraine, Bulgaria, Latvia, Lithuania, Estonia and other countries form the largest professional team of medical writers in the region. We are also happy to prepare the documents for drugs trials in Estonia, Georgia and the USA.
The sponsor is free to choose the way of interaction with OCT regarding medical writing in Russia. It can be provided as a stand-alone service as well as it can be a component of the project conducted by a full-service CRO in Central and Eastern Europe (CEE).
There are only qualified translators in OCT staff, who work strictly in accordance with corporate standard operating procedures (SOP). We also have a team of outsourced translators, whose quality of work was proved by the successful experience.