As a candidate for EU membership, Turkey has aligned its medical device regulations closely with those in the EU. The Turkish Ministry of Health regulates medical devices in the country, and requires CE Marking for all devices imported into Turkey. Manufacturers must also have proof of conformity to EU requirements and register in the TITUBB database in order to sell them in the Turkish market.
Let Emergo assist you in evaluating the Turkish medical device regulatory framework as it applies to your device(s)
Emergo's worldwide network of consultants, industry contacts and regulatory sources enables us to develop in-depth and accurate analysis of multiple medical device markets such as Turkey.
Our Global Regulatory Overview report service covers various aspects of the Turkish medical device market, including:
- Regulatory Background of the Turkish Ministry of Health
- Product Assessment
- In-Country Representation in Turkey
- Medical Device Registration Requirements
- Costs and Timeframes
- Labeling and Language Requirements
- Turkey Regulatory Roadmap
Please contact us for more information about our Regulatory Overview Report for Turkey.