Understanding Document Registration for Medical Devices in Turkey
An Overview of Document Registration for Medical Devices in Turkey
In Turkey, document registration is a crucial step in obtaining Regulatory approval for medical devices. The Türkiye İlaç ve Tıbbi Cihaz Kurumu (TITCK), or the Turkish Medicines and Medical Devices Agency, oversees this process, ensuring strict adherence to the country’s regulations and standards. Manufacturers and importers must undergo a comprehensive evaluation prior to introducing their devices in the Turkish market.