Clinical trial protocols, Ministry of Health regulatory submissions, pharmaceutical dossiers, and patient materials translated by Turkish medical specialists.
Turkey has one of the fastest-growing healthcare markets in the world, supported by a large young population, expanding private hospital networks, and significant government investment in public health infrastructure. The Turkish Medicines and Medical Devices Agency (TITCK) regulates pharmaceutical and medical device approvals, with specific Turkish-language documentation requirements. Our Turkish medical translators hold degrees in medicine, pharmacology, or life sciences and are fully fluent in TITCK submission standards.
In-depth knowledge of Turkish Medicines and Medical Devices Agency submission requirements for drug registration and medical device marketing authorization.
Translation, editing by a second Turkish medical linguist, and a final terminology check against validated Turkish medical glossaries.
Every Turkish medical project is handled by a translator with a proven background in medicine, pharmacology, or life sciences.
We support international healthcare companies entering the Turkish market with full dossier translation and patient communication materials.
“We are extremely satisfied with the translation services provided. The translations were accurate, professional, and delivered on time. The attention to detail and linguistic precision were outstanding. Communication was smooth, and the team was always +”
Google review (INTL) , a year ago
“I recently used a translation agency in France to translate several administrative and commercial documents into Spanish. The service I received was absolutely exceptional. Not only were the translations accurate and professional, but the team was also very +”
Google review (FR) , 2 years ago
“They offer great and reasonable prices for sworn translations. Thank you for your help in translating my documents for my legal process.”
Google review (SL) , 6 months ago
Yes. We produce Turkish-language dossiers for TITCK drug registration and medical device marketing authorization, following the Agency's specific formatting and terminology requirements.
Yes. We translate clinical trial protocols, investigator brochures, and patient-facing materials for Turkish clinical sites, ensuring compliance with Turkish Ministry of Health ethics committee requirements.
We build client-specific Turkish medical glossaries and translation memories at project start and maintain them throughout the full regulatory dossier lifecycle.
Yes. Turkey's Medicines and Medical Devices Agency (TITCK) requires specific Turkish-language document structures and terminology for drug and device registrations. Our translators apply TITCK-specific terminology conventions for drug classification, dosage terminology, adverse event reporting, and device risk categories. For products following the parallel EU MDR pathway we also apply EU technical file requirements where TITCK accepts mutual recognition.
A standalone Turkish informed consent form of 2,000 to 4,000 words typically delivers in 2 to 3 business days including QA. A full investigator brochure or 50-page TITCK registration module runs 5 to 10 business days. Turkish text typically expands 15 to 20 percent over English source due to agglutinative word formation; factor this into page count estimates. For multi-country studies running Turkish in parallel with other language versions we assign a dedicated project manager to align all timelines.
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