Clinical trial protocols, patient information materials, pharmaceutical dossiers, and regulatory submissions translated by Russian medical specialists.
Eastern Europe and the CIS region are significant markets for pharmaceutical clinical trials and medical device registration. Russia operates its own regulatory authority (Roszdravnadzor), and Kazakhstan and Ukraine each have distinct national requirements. Our Russian medical translators hold degrees in medicine, pharmacy, or life sciences and understand the submission standards across all three regulatory environments.
Every Russian medical project is handled by a translator with a proven background in medicine, pharmacology, or life sciences, not a general-purpose linguist.
Translation, editing by a second medical linguist, and a final terminology check against validated Russian medical glossaries and WHO INN lists.
Familiar with Russian federal health regulations and Eurasian Economic Union (EAEU) pharmaceutical registration requirements.
Patient information leaflets and informed consent forms receive additional review to ensure terminology is accurate and accessible to Russian-speaking patients.
“Reliable, trustworthy and customer-centric This is the summation of Michael, Suzy and their team of translators. I have worked with them for over a year, and they have been my translation service for advertising in many European languages - from Swedish to German to Russian, and not always from English! Consider them a rare find.”
Google review (INTL) , 6 years ago
“Excellent service and good value translation company! Efficient, accurate, and fast turnaround at competitive rates. Highly recommended for their outstanding communication and prompt responses on the chat.”
Google review (SL) , 2 years ago
“It is a real pleasure to work with the BeTranslated team who has been very professional, flexible and responsive during all projects.”
Google review (INTL) , 3 years ago
Yes. We have experience with Russian Federal Service for Healthcare Supervision submissions and follow the formatting requirements for Russian drug registration dossiers.
Yes. We have the capacity to manage multi-country projects with a single project manager coordinating across all CIS trial sites, ensuring consistent terminology and formatting.
We build client-specific Russian medical glossaries and translation memories at project start. These assets are maintained and updated throughout the project lifetime, ensuring consistency whether the dossier runs to 200 or 2,000 pages.
Yes. Russia's Federal Service for Healthcare Supervision (Roszdravnadzor) and the Eurasian Economic Union (EAEU) pharmaceutical registration framework each have specific Russian-language document structures and terminology conventions. We follow Roszdravnadzor CTD formatting guidance and EAEU TR 043/2017 technical regulations for medical device documentation. Our translators apply the correct official terminology for drug names, dosage units, adverse event classification, and clinical trial phase descriptions throughout.
All translators and project managers sign GDPR-aligned data processing agreements before receiving any patient-identifiable or trial-confidential material. Files are transferred over encrypted channels, processed on secure infrastructure outside Russian jurisdiction, and purged from our systems on project closure unless you request translation memory retention. For projects involving Russian patient data subject to Federal Law 152-FZ (On Personal Data) we flag handling requirements at project start.
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