TR 
EN 
A Pre-Authorization Guide is published by the Turkish Medicines and Medical Devices Agency (“the Agency”) regarding the pre-authorization processes that have been required for the export and import of certain medical products as stipulated by the following communiques:
“Communique on the Amendment of the Communique on Export-Prohibited and Pre-Approved Goods” published in the Official Gazette No. 31058 dated March 3, 2020 (please see for further information: http://herdem.av.tr/corona-outbreak-turkey-to-control-export-of-medical-masks),
“Communique on the Amendment of the Communique on Export-Prohibited and Pre-Approved Goods” published in the Official Gazette No. 31080 dated March 26, 2020” (please see for further information: http://herdem.av.tr/corona-outbreak-turkey-to-control-export-of-intensive-care-medical-equipment) and
“Import of Medical Diagnostic Kits No. 2020/19” published on the Official Gazette No. 31087 dated April 2, 2020 (please see for further information: http://herdem.av.tr/corona-outbreak-communiqu-on-the-import-of-medical-diagnostic-kits).
Additionally, the Agency stated that the purpose of this guide is to help companies to adapt the regulations and to run this process more effectively.
You can find the guide via link:
