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Amendments to align the regulations with existing EU standards on medical devices and in vitro diagnostic devices, ensuring their applicability in Türkiye, were published on August 17, 2024.

Türkiye İlaç ve Tıbbi Cihaz Kurumu ("TİTCK"), Çeşitleme Başvuruları ile Varyasyon Başvurularının Sınıflandırılmasına Dair Kılavuz'u ("Kılavuz") 14 Nisan 2022 tarihinde yayımladı.

All kinds of manufacturing, marketing, and after-sales activities of medical devices are highly regulated in Turkey. The main framework for ensuring safety and compliance with the technical specifications is governed by the Law on Product Safety

The Turkish Constitutional Court's Decision No. 2018/6707, dated 31 March 2022, regarding the violation of a doctor's freedom of expression was published in the Official Gazette on 26 May 2022.

11/03/2024 tarihli ve 32487 sayılı Resmî Gazetede yayımlanan;

This matter started as an ordinary anti-counterfeiting case after receiving a picture of a fire-resistant glass from a global manufacturer of such products.

Private healthcare emerged in Turkey as a result of the long lines and poor medical services associated with state-run hospitals.

The advertisements and promotions pertaining to hygiene and health care products have increased in number in parallel with the necessities arising due to the COVID-19 pandemic.

In its decision dated 14th of July 2020 the Advertisement Board imposed sanction against the advertisement of a food supplement branded "No Attack".

Pharmaceutical prices in Turkey have always been one of the most controversial issues. The prices of medicines that are to be marketed are set in accordance with the Decision ...

The Decree Numbered 703 Amending Certain Laws and Decrees for the Purposes of Compliance with the Amendments to the Constitution was published in the 3rd repeating Official Gazette dated 9 July 2018 and numbered 30473.

The Guideline prepared by the Turkish Medicines and Medical Devices Agency ("Agency") has been updated and published on the official website of the Agency.

Turkey's pharmaceutical regulatory landscape has evolved with new naming guidelines for human medicinal products. The Turkish Medicines and Medical Devices Agency has established comprehensive procedures for assessing product name similarity, incorporating INN root analysis and automated screening systems. These regulations introduce structured evaluation criteria and appeal mechanisms that will reshape how pharmaceutical companies approach product naming in the Turkish market.

The Legislative Proposal on the Amendment of the Law on Pharmaceuticals and Medical Preparations No. 1262, Certain Laws and Decree Law No. 663 ("the Legislative Proposal") dated March 20, 2023...

The Turkish Medicine and Medical Devices Authority ("TITCK") recently issued a new Medical Devices Regulation (the "New Regulation") revising the main framework governing the safety, marketing and clinical studies of medical devices.

Due to the rapid increase in the current exchange rates, pharmaceutical prices have been one of the most controversial issues in Türkiye in 2023.

The Turkish Pharmaceuticals and Medical Devices Authority (TİTCK) recently announced that the draft amendments to the Regulation on Clinical Trials of Pharmaceuticals and Biological Products ("Regulation") ...

Regulation on Products Derived from Human Tissues and Cells and Centres Related to These Products ("Regulation") has been published in the Official Gazette number 33007 dated 4 September 2025, and by the Ministry of Health.