Ministry of Health Publishes a Draft Regulation on Amending Turkish Biocidal Product Regulation

Date
31 Aug 2021

Biocides Human health exposure Labelling Product authorisation Permitting or licensing

GPC - Global Product Compliance

The Ministry of Health, Turkey published on their webiste the draft regulation on the amendment of Turkish Biocidal Product Regulation.

 Current Biocidal regulation came into force on 31.12.2009 in Turkey. The regulation aims to assess the effects of biocidal products on humans, animals, and the environment while regulating the classification, labeling, packaging requirements, exports, licensing for biocidal products, and conditions for putting products into the market.  

To prevent confusion and to make regulation more practical, this draft is prepared to amend articles regarding application for license and registration and definition of the authorized laboratory. With this amendment, this regulation will be in line with European Union Biocidal Regulation. According to this amendment, pre-application is no longer needed, and the definition of the authorized laboratory has been changed. 

 Interested people can submit their opinion through an official form to hsgm.cevre@saglik.gov.tr by 10.09.2021.