19 Nov 2024
The Regulation on the Withdrawal of Medicinal Products for Human Use and Foods for Special Medical Purposes was published in the Official Gazette dated October 23, 2024 and numbered 32701 and entered into force as of the date of […]
17 Aug 2023
On 23.06.2023, The Guide on Packaging Information and Readability of the Package of Foods for Special Medical Purposes was published on the website of the Turkish Medicines and Medical Devices Agency. The Guide is prepared in accordance with the […]
21 Jul 2023
The Regulation covers the market control activities of (i) the human medicinal products that are licensed or authorized by the Agency, (ii) the active substances used in their production, (iii) foods having special medical purposes. Magistral medicines are not […]
21 Jul 2023
The Regulation on Inspection of Health Claim (“Regulation“) was published in the Official Gazette by the Turkish Medicines and Medical Devices Agency (“Agency“) and entered into force on 13 June 2023. With the entry into force of the Regulation, […]
23 Jun 2023
The Guideline on Import Applications and Marketing Authorization (“Guideline“) prepared by the Turkish Medicines and Medical Devices Agency (“Agency“) and entered into force on 29 August 2022 has been updated. The updated Guideline entered into force on 05 June […]
9 May 2023
Regulation on Procurement of Medicines from Abroad (“Regulation”) was published in the Official Gazette on 03.02.2023 by the Turkish Medicines and Medical Devices Agency and entered into force in the same day. The Regulation was prepared in parallel with […]
9 May 2023
The purpose of the Guideline is to determine the procedures and principles regarding the withdrawal and recall of medical devices and in vitro diagnostic devices from the market, and the duties, authorities and responsibilities of Turkish Medicines and Medical […]
9 May 2023
Regulation on Licensing of Medicinal Products for Human Use (the “Regulation”) has been published in the Official Gazette number 31686 and dated 11 December 2021 to ensure security and quality of medicinal products for human use, to determine the […]
6 Apr 2023
The amendment regarding the Guide on License Renewal for Human Medicinal Products (“Guide”), prepared by the Ministry of Health, Turkish Medicines and Medical Devices Agency within the scope of Article 21 of the Regulation on Licensing of the Human […]
