We empower global medical device manufacturers and distributors to seamlessly enter and scale in the Turkish healthcare market. From company setup and UTS registration to public procurement (DMO & EKAP) — we manage your full regulatory lifecycle
Our services allow you to build your own way to access the Turkish Medical Market



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Entering the Turkish healthcare market involves complex regulatory and operational hurdles. Here is how we streamline the process for foreign manufacturers


Find quick answers regarding TITCK compliance, UTS product registration, and DMO Health Market cataloging processes.
Strategic Public Procurement Guidance for International Medical Device Manufacturers
Direct access to 800+ public hospitals, guaranteed payment terms, and streamlined public procurement pathways across Türkiye’s healthcare network.
Before applying for DMO listing, foreign medical device manufacturers must fulfill specific local compliance steps to ensure a seamless approval process.
A clear, structured roadmap to register your medical devices on the Turkish State Supply Office (DMO) catalog and access public hospital procurement.
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Headquartered in Ankara — direct proximity to DMO and the Ministry of Health.
Zero-hassle execution of complex regulatory workflows, licensing, and public healthcare tenders.
Faster time-to-market with dedicated local regulatory and operational expertise.
Stay updated on the latest TITCK announcements, UTS compliance shifts, and DMO Health Market regulations affecting medical device manufacturers.