Our Services
Our services focus on aligning regulatory requirements with real operational needs in Türkiye’s medical device sector.
In many cases, compliance exists, and operations are in place — yet the connection between them is missing.
We work to bridge this gap by building structured, practical systems that function not only on paper, but in everyday operations.
Product Registration & UTS Processes
Supporting medical device companies in Türkiye with product registrations and UTS processes, from initial setup to ongoing updates.
Resolving common issues that delay product availability and ensuring alignment between regulatory requirements and operational execution.
DMO Process Alignment
Aligning UTS, regulatory, and operational processes with DMO requirements.
Ensuring smooth execution across pricing, documentation, delivery, and invoicing.
Supply Chain & Field Logistics
Managing stock planning and field distribution for medical devices, including last-minute and surgery-based demands.
Ensuring that products are available at the right place and time, supported by structured and responsive logistics systems.
Import & Customs Coordination
Coordinating import and customs processes for medical devices, with hands-on experience in hearing systems and related technologies.
Supporting smooth product entry into Türkiye by aligning regulatory requirements, documentation, and operational timelines.
Ensuring efficient clearance and readiness for distribution without delays.
If your regulatory and operational processes are in place but not working as expected, feel free to reach out. We are always open to discuss your current setup and explore practical ways to improve it.