M.Sc.in biophysics, Ph.D.in biochemistry
I work for leading translation agencies translating such documents as:
» registration dossiers
» clinical trial protocols
» drug safety reports
» summaries of product characteristics (SPC)
» user manuals for pharmaceutical lab. & medical equipment
» interfaces for pharmaceutical software
» marketing brochures
» IFUs
» lab reports
» packaging and labels
» informed consents
» patients diaries
» questionnaires

Nonclinical toxicology study reports, pre-clinical safety profiles, fertility and embryo-fetal development study, PK data, PD data, treatment emergent AE’s, treatment related toxicity, safety summary, response summary, ICF/PIS, SUSAR, SAEs reports, CIOMs, investigator brochures, protocols and protocol amendments, case report forms, lab manuals, e-diary instructions, imaging guideline manuals, annual safety reports, initiation visits, medical monitor visits, sponsor audits.

Medical translation is serious business. Mistakes can be a matter of life or death. As such, it requires a keen focus on accuracy and terminology. And I deliver exactly that.
I have 15-year translation experience and medical education so whether you are submitting dossier for pharmaceutical registration, localizing software, translating clinical trial materials or documentation for global sales of medical equipment I can produce localized medical documents of the highest quality on the market.

Clinical trial protocols, informed consents, investigator brochures, drug safety reports, patient information leaflets, user manuals for medical equipment, lab reports, informed consents, patient's records, software interfaces for clinical assessments. Full time medical interpreter for 13 years. Completed a medical terminology college course, "Bridging the Gap" medical interpreter training program, and Design and Interpretation of Clinical Trials course authorized by Johns Hopkins University.

The clinical trial of rivaroxaban

Experienced in translating pharmaceutical documentation since 2014. Specialized in translating POMRs, medical history records, patient information leaflets, discharge summaries, medical tests, mental status examinations, hospital reports, operation reports, informed consent forms, CT Scans, PET Scans, MRI Scans and ultrasound reports, radiology reports, pathology reports, laboratory reports.

Over the past decade, I have performed most of the linguistic tasks in the end-to-end Clinical Trial Solutions, incl. the full cycle of pharmaceutical product development from Preclinical to Phases I-III stages:
• Clinical Trial Materials & Filings (PISs/ICFs, IBs)
• Pharmacovigilance & Safety (IRB/EC/IEC comm., SAEs, SUSARs)
• Drug Discovery & Development (export/import)
• Compliance & Regulatory (Phase IV/Sales, MAAs, EMA/FDA Comp.)
• Product Marketing & Launch (CSRs, SmPCs, FSNs, SmPCs)

I am a professional, Russian-native translator with a Specialist Diploma in Linguistics & Translation (with Honors), which is equivalent to a master's degree in the US.
I have over 10 years' experience in medical/pharmaceutical translation, specializing in clinical studies (patients' info and consent, protocols/amendments, ICFs), medical devices (operating instructions, (contra)indications), clinical study agreements, and drugs (description, label info, certificate of analyses/conformity).

I am a pharma/medical translator with a strong scientific background: Ph.D. in biochemistry, theoretical and practical experience in academy. I specialize in the translation of pharma documents, including clinical research documentation; pharma documents; patents and patent applications related to pharma and biotechnology; scientific papers. I participated (as a translator, editor, reviewer, and proofreader) in many projects: ~3.2 mln words translated, and ~1.3 mln words edited.

Being a medical doctor and linguist with 9+ years translation and localization experience and 14 years in life sciences, I help language service providers, medical, pharmaceutical and biotech companies, contract research organizations, publishing houses, government and non-government organizations translate medical, pharmaceutical, clinical trials, veterinary and life sciences documentation from English to Russian, English to Ukrainian, Russian to English, Ukrainian to English.

My way in pharmaceutical translations started like the way of our ancestors in pharmaceutics — from herbs. Being interested in Ayurveda, I was acquainted with Indian Pharmacopoeia and Traditional Medicine. However, I live in the modern world and translate pharma-related documents for global pharmaceutical companies. I stay in touch with news both in current plant-based health supplement developments and in pharmaceutical breakthroughs.

Types of most common translation/editing projects:

Clinical Study Protocols,
Investigator’s Brochures,
Informed Consent Forms,
Safety Reports,
Instructions for Use,
Pharmaceutical Articles & Papers,
Pharmaceutical Employee Handbooks & Newsletters,
etc.

I am a biologist and I studied human physiology extensively.
My pharmaceutical translation experience started in 2011 when I was hired to work as a translator and interpreter at the quality assurance department at Synbias Pharma Ltd. (Donetsk, Ukraine). In 2014 I quit the position and became a pharmaceutical freelance translator to be able to translate for other pharmaceutical companies in the world.
Before 2011 I translated for M.Gorky Donetsk National Medical University.

Pharmaceutical translation is one of my main areas of specialization. I can help you if you need to translate:
- common technical documents (CTD);
- periodical safety update reports (PSUR);
- summaries of product characteristics (SmPC);
- patient information leaflets (PIL);
- certificates of analysis (CoA);
- case report forms (CRF);
- clinical trial protocols;
- questionnaires;
- training texts;
- scientific articles;
- texts on homeopathy and natural remedies.

• clinical trials/pharmaceutical industry (CTAs, protocols, investigator CVs, IRB/IEC opinions, IBs, ICFs, patient information sheets, diaries, questionnaires, PROs, RA correspondence; analytical procedures, CoAs, CPPs, DMFs, GMP certificates, MIAs, PILs, PSURs, SMPCs, SOPs, labels, validation reports)
• medical devices (diagnostic/surgical tools, lab equipment)
• medical records (case records, certificates, diagnostic findings)
• public health (brochures, flyers, guides, leaflets, posters)

Study Protocols, Patient Information Sheets, Informed Consent Forms, Investigator’s Brochures, Patient Instructions, Study Participant Guides, Questionnaires, Doctor to Patient Letters, Patient Cards

I am a native Russian speaker and an English to Russian and vice versa medical translator/editor with over 27 years of experience. I graduated from 2nd Moscow Medical Institute with a degree Physician-Biochemist and later got a PhD in Biochemistry. For the last 9 years, I have been working as a medical editor and translator in a medical translation agency in Moscow and was engaged in editing and translation of the content from most of the pharmaceutical companies in Russia.

I specialize in medical and pharmaceutical translation, and have master’s degree in translation. Up to this date, I’ve been translating clinical trial agreements, clinical trial protocols, investigator’s brochures, informed consent forms, patient-facing questionnaires, letters to regulatory authorities, certificates of analysis, declarations of conformity, instructions for use, labels.

Medical trial materials for traditional and non-traditional (ayurvedic) pharmaceutical products, inserts to pharmaceutical products, packing equipment for pharmaceutical products (vials) and marketing materials.

Translation of non-clinical and clinical trials, data sheets, certificates of analysis, PSURs, instruction leaflets, articles etc.

Doctor of veterinary medicine
SFT (Société française des traducteurs) membre
Examples of documents translated: Common Technical Documents (CTD), Summary of product characteristics, Drug labels, Specifications, Package leaflet: information for the user, Clinical overview, Training materials, marketing research, manuals, patient medical records, certificates of conformity...

Jobs handled
- Translation of product registration dossiers to include product composition, indications, contraindications, pharmacology, pharmacokinetics, quality control, adverse drug reports, manufacturing processes, presentation etc.
- Translation of clinical trial protocols and reports
- Translation of literature of primary and secondary packaging material
- Translation of research material
-Translation of marketing material

I hold a Bachelor of Physiotherapy from the University of Melbourne and have worked as a physiotherapist for over 7 years. I have worked as a translator and editor for over 5 years, specialising in clinical trial documentation, journal articles, product catalogues for biomedical and pharmaceutical companies, and medical website content. I am a NAATI Certified Professional Translator (Russian to English).

I am able to provide quality and accurate translation in the pharmaceutical field beacause I know how to search necessary information and how to communicate data clearly.
Professional translator for 10 years. Certified translator.
My translation skills have been audited and approved by OTTIAQ, a Canadian translation authority in Quebec.

I have completed various projects in pharmaceutical and medical fields.

I have MA in English language and literature and I specialize in medical translations from English into Russian and Ukrainian for more than 20 years. I am translating on a daily basis the documents in medical/pharmaceutical field including protocols of clinical studies, informed consent forms, investigator brochures, drug inserts and labels, medical records, EMA papers, etc. Total amount of words translated in medical/pharmaceutical field is ~7 million.