NDB – National DataBank
REPUBLIC OF TURKEY MEDICAL DEVICES AND DRUGS DATABANK
Registration Company and Products to Medical devices & Drugs databank process
Turkey Pharmaceuticals and Medical Devices National Data Bank (TİTUBB) system for the implantable medical devices, in vitro National Data Bank of medical devices used ‘the record whether the ministry will cover the process of approval of eligible products. The recording will be shown in Turkey as a result of medical devices approved in a public inquiry.
Why is it necessary?
- Companies that import or manufacturers of devices under the Medical Devices Regulations; necessary information about the company and documentation of medical devices and must notify the Databank agency.
- If the manufacturer of medical devices outside the borders of the country; legal representatives, importers, distributors, and medical device companies must report the necessary information and documents related to the Authority.
- Medical devices placed on the market during the which is required to be registered on (TİTUBB) Republic of Turkey National Drug and Medical Device Data Bank of medical devices.
Which documents are required for registration?
Get in contact with us about the required documents for registering companies, you can make the system inquiry. The list of necessary documents according to the information in the system we can share with you.
Consult our experts for your product registration, you can provide a list of documents required for registration of the product according to your property.
Our other services you can get at Databank system
- Databank Dealer registration / admission process
- Databank Document Registration and Update Process
- Databank Product Registration and Update Process
- Republic of Turkey Social Security Institution Registration
- Getting Databank Free Sales Certificate
By firms wanting to export products covered by the regulations of the National Data Bank Turkey Pharmaceuticals and Medical Devices (TİTUBB) then registration is completed the Free Sales Certificate (Declaration) should be filed.
Exporting companies, products that are produced in accordance with the directives and regulations relating to products in Turkey declares that it does not pose a risk to human health if used properly.
Our team of professional experts doing for product documentation and upload to system, properly registration, follow-up and submitted to the ministry performs the process as quickly and easily.
Note: Pro Danışmanlık provide support for the provision or execution that in International English / Italian / Bulgarian languages by the necessary documents and process for foreign companies.