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The Pharmaceutical and Medical Device Authority's approval is now required for health declarations used on food and food supplement labels, or in promotions and advertisements.

The protection of personal data (including personal health data) is regulated under Personal Data Protection Law ("DPL") numbered 6698.

The amendment defines the existence of the conditions set forth in paragraph three of Article 6 of the LPDP as the principal rule governing access to personal health data.

The Regulation on the Promotional Activities of Medicinal Products for Human Use ("Regulation") defines the scientific and product promotion meetings and regulates how the marketing authorization holders...

Medical device quality management system in Turkey has been quickly changing over the years. Besides, the legal and political environment on medical device quality management systems...

The Amendment mostly clarifies the inconsistencies and removes the burdensome obligations created with the Regulation as expected.

lgili kişinin 2018 yılı Ocak ayında hastanede bir doktor tarafından muayene edildiği, ilgili doktorun hastaneden ayrılarak özel muayenehane açtığı, akabinde cep telefonu numarasına...

The Turkish Pharmaceuticals and Medical Devices Authority (TİTCK) has published announcements on the testing, control and calibration of medical devices as well as the...

The Turkish Pharmaceuticals and Medical Devices Authority ("TİTCK") has published announcements on the amendments to the regulation on cosmetic products, licensing homeopathic medical products and ...

Medical malpractice encompasses preventable healthcare errors that cause serious harm to patients. Understanding common examples—from misdiagnosis and surgical mistakes to medication...

By its very nature, public trust in healthcare professionals ("HCPs") is at the heart of the patient – HCP relationship and is crucial for the continuity and reliability of healthcare services.

Turkey's position as a bridge between the leading European cosmetic companies, and Asian and Middle East countries where there is a high demand for cosmetic products is significant.

It is clear that the matter of malpractice is still the main challenging issue for every single malpractice lawyer in Turkey.

Amendment to the Regulation on the Licensing of Medicinal Products for Human Use. An amendment to the Regulation on the Licensing of Medicinal Products for Human Use has been introduced on 3 December 2024.

In 2014, the Turkish Medicine and Medical Device Institution's ("Institution") New Year's resolution list included two remarkable items: (i) ensuring people's access to safe human medicinal products, and (ii) battling the grey economy.

Regulation on Products Derived from Human Tissues and Cells and Centers Concerning These Products was published in the Official Gazette dated September 4, 2025 and numbered 33007.

Turkey's Ministry of Health has introduced significant changes to its health information management systems regulations, removing several certification requirements and streamlining registration procedures for service providers. The amendments eliminate mandatory CMMI and SPICE certifications while expanding deletion penalties and modifying procurement processes, fundamentally reshaping compliance obligations for healthcare technology vendors operating in the Turkish market.