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Devices Agency has updated the Guideline on the Scheduling Processes for Marketing Authorization Applications of Medicinal Products for Human Use, the Guideline on Biosimilar Medicinal Products, and the Guideline on the Importation of Medicines from Abroad

29 Aug 2024

One of the most significant updates in the Guideline on the Scheduling Processes for Marketing Authorization Applications of Medicinal Products for Human Use (“Scheduling Guideline”) is the new regulations regarding hybrid applications. Firstly, the Scheduling Guideline has been updated […]

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Amendments regarding the Guide on License Renewal for Human Medicinal Products, made by the Ministry of Health, Turkish Medicines and Medical Devices Agency were published on the official website of the Ministry of Health.

21 Jul 2023

Turkish Medicines and Medical Devices Agency (“Agency”) has published amendments to the Guide on License Renewal for Human Medicinal Products (“Guide”) on 18.05.2023 which was prepared within the scope of Article 21 of the Regulation on Licensing of the […]

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