Team
TRANSLATIONS TO RUSSIAN
The following is an overview of our specialised medical translators who are Russian native-speakers. They are paired with a trusted colleague with whom they regularly cooperate on projects requiring translation and revision using the four-eyes principle.
Irina Smirnova
Source languages
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English
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Latvian
Services
Translation ▪ Copy-editing ▪ Proofreading ▪ Implementation of changes ▪ Linguistic validation ▪ Correction of proofs
Specialisms
Life sciences and medical translations: clinical trial protocols, patient information leaflets, informed consent forms, investigator brochures, regulatory submissions, medical device manuals, labeling, pharmacovigilance reports ▪ Legal documents: contracts, powers of attorney, certificates ▪ Marketing materials: brochures, product catalogs, newsletters, email campaigns, social media posts, digital ads, presentations, case studies, event materials, press releases, landing pages, webinars, product sheets, testimonials
Deniss Gamezo
Source languages
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English
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German
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Latvian
Services
Translation ▪ Revision ▪ Editing ▪ Implementation of changes ▪ Localisation ▪ Back-translations ▪ Harmonisation ▪ Linguistic validation ▪ Cognitive debriefing (without recruitment) ▪ Linguistic sign-off (LSO) ▪ Subtitling ▪ Testing apps ▪ Electronic implementation/migration ▪ Screenshot reviews ▪ Drawing up glossaries ▪ Transcription
Specialisms
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Clinical trial documents for patients, such as informed consent/assent forms, patient diaries, patient questionnaires, (e)PROs, (e)COA, patient recruitment materials and lay protocol synopses
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Clinical trial documents for healthcare professionals, such as investigator’s brochures (IBs), research protocols and protocol synopses
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Regulatory pharmaceutical documents, such as summaries of product characteristics (SmPCs), labels and patient information leaflets (PILs)
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Medical device documents, such as instructions for use (IFUs), manuals, summaries of safety and clinical performance (SSCPs), software user guides, standard operating procedures (SOPs) and laboratory manuals
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Legal documents, such as clinical trial agreements and marketing authorisation documents (including DSURs and PSURs)
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Protected health information (PHI), such as medical records, hospital admission and discharge reports and lab reports