Pharma & Health
Cosmetic Products Regulation
The Cosmetic Products Regulation, published in the repeated issue of Official Gazette No. 32184 of 8 May 2023, regulates the procedures for cosmetic products made available on the market in order to ensure a high level of protection of human health (Article 1). It is based on Law No. 7223, Article 7 of the Cosmetics […]
Medical Device Regulation
The Medical Device Regulation (Tıbbi Cihaz Yönetmeliği), published in the repeated issue of Official Gazette No. 31499 of 2 June 2021, sets the procedures for placing medical devices for human use and their accessories on the market, making them available and putting them into service, on the basis of a high level of protection of […]
Regulation on the Recall of Human Medicinal Products and Foods for Special Medical Purposes
The Regulation on the Recall of Human Medicinal Products and Foods for Special Medical Purposes, published in Official Gazette No. 32701 of 23 October 2024, sets the rules, powers and responsibilities for investigating products that are suspected of being defective, found defective or considered unsafe to use, and, where necessary, for withdrawing them from the […]
Regulation on Market Control of Human Medicinal Products and Foods for Special Medical Purposes
The Regulation on Market Control of Human Medicinal Products and Foods for Special Medical Purposes, published in Official Gazette No. 32729 of 21 November 2024, sets the procedures, powers and responsibilities for planning, carrying out and evaluating the market control activities that keep products licensed or authorised by the Turkish Medicines and Medical Devices Agency […]
Regulation on the Control of Medical Waste
What does the Medical Waste Control Regulation cover? The Medical Waste Control Regulation was published in the Official Gazette dated 25 January 2017, No. 29959. It governs the separate collection of medical waste generated by healthcare facilities at source, its transport within the facility, temporary storage, transport to the treatment facility and disposal (Articles 1 […]
Destruction of Human Medicinal Products: Legal Framework
Is the destruction of human medicinal products governed by a single regulation? No. There is no single regulation called a "destruction procedure" for expired or unusable human medicinal products; the process is made up of complementary instruments. Tracking and the product's record in the system are governed by the Pharmaceutical Tracking System (İTS), operated by […]
Hizmet
Pharmaceuticals
Safe, documented and officially witnessed waste disposal of expired, recalled, or excess pharmaceutical stock.
Hizmet
Medical Devices
KVKK-compliant data wiping and official de-registration from the UTS registry, followed by waste disposal of end-of-life or faulty medical devices.
Post
Medical Device Recall (FSCA) and Disposal of Field Stock
How a medical device recall differs from an FSCA, the duties of the manufacturer, importer, and distributor, the reporting deadlines, and the disposal steps.
Post
We Sponsored the Medical Device Governance Summit 2.0 and Gave 1,300 Saplings to the Future
We sponsored the Medical Device Governance Summit 2.0 on 10–13 May 2026 and gave a total of 1,300 saplings to the future with A Breath for the Future, A Tree in Your Name.
Post
Medicine Recall and Expired Medicine Disposal: Steps for the License Holder and the Warehouse
Classes, the 24-48-72 hour deadlines, the duties of the license holder and the warehouse, health directorate verification, and disposal in a medicine recall.
Post
The Danger of Fake Vitamins Sold Online: atv News Report
atv Haber reports on the risks of fake vitamins and supplements sold online. What should you check on the label, and what should producers do?