DRAFT OF THE REGULATION AMENDING THE TURKISH BIOCIDAL PRODUCTS REGULATION IS PUBLISHED
Ministry of Health of Turkish Republic published the Draft of the Regulation Amending the Biocidal Products Regulation for the purpose of consultation of the stake holders.
The Draft Regulation contains important revisions including the below listed subjects;
- Assigning the Institute of Medicine and Medical Devices of Turkey as the Competent Authority for Biocidal Products Product Type-1 and Product Type-19 which are in direct contact with the human body,
- Adaptation of the revisions in the regulations which are published by Ministry of Environment and Urbanization (such as SEA, SDS Regulations) to the Biocidal Products Regulation,
- Adaptation of some definitions from the EU BPR (528/2012/EU) into Turkish Legislation for the alignment of the regulations and to prevent conflicts and ambiguity,
- Improvements for some issues causing challenges on the process, including the extension for the validities of the inventory notification approvals.
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