On 9 September 2021, the Medicines and Medical Devices Agency published the draft Licensing Regulation on Homeopathic Medicinal Products (Turkish language) (Draft Regulation). The purpose of this regulation is to regulate the procedures and principles to be applied in licensing, packaging and distributing homeopathic medicinal products, which have protective, supportive or curative effects on human health, to ensure their effectiveness, safety and quality.
The Draft Regulation was open to public consultation until 20 September 2021. It is unknown when the Draft Regulation will be published in the Official Gazette and enter into force. If passed, it will be the first regulation to be made in this field.
First published by Practical Law, in 04.10.2021