“Excellent service and good value translation company. Accurate, fast turnaround at competitive rates. Highly recommended for their outstanding communication and prompt responses.”
Claire C.
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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.
Client Reviews
“Excellent service and good value translation company. Accurate, fast turnaround at competitive rates. Highly recommended for their outstanding communication and prompt responses.”
Verified Google Review
“The team was meticulous with scientific and academic terminology. They delivered a flawless translation of my doctoral thesis on time, and communication throughout was outstanding.”
Academic Translation Client
“My experience with BeTranslated was great. They respond quickly and I recommend the agency 100%.”
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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.
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