How is Biocidal Product Licensing Done?

For the biocidal product licensing process to be completed, the steps outlined in the Biocidal Products Regulation must be followed in full, the license application must be submitted to the ministry, and approval must be obtained.

The Biocidal Products Regulation is the fundamental legal framework, but there are many other legal regulations that must be considered. These include:

•    Biocidal Products Regulation (Official Gazette No. 27449, 4th Supplement, dated December 31, 2009)
•    Regulation Amending the Biocidal Products Regulation (Official Gazette No. 28149 dated December 21, 2011)
•    Regulation Amending the Biocidal Products Regulation (Official Gazette No. 28939 dated March 12, 2014)
•    Regulation Amending the Biocidal Products Regulation (Official Gazette No. 31066 dated March 12, 2020)
•    Regulation on Amendments to the Biocidal Products Regulation (Official Gazette No. 31705 dated December 30, 2021)
•    Regulation on the Classification, Labeling, and Packaging of Substances and Mixtures (SEA) dated December 11, 2013, No. 28848
•    Regulation on the Registration, Evaluation, Authorization of Chemicals (KKDİK) dated June 23, 2017, No. 30105 (Repeated)
•    INSTRUCTION ON PRODUCT TYPE-1 AND PRODUCT TYPE-19 BIOCIDAL PRODUCT ANALYSES published with Official Gazette No. 3949 dated March 5, 2021
•    Instructions on Biocidal Product Analyses and Authorized Laboratories, updated by Official Decision No. 3851 dated 23/09/2021