The Instruction on Biocidal Product Analyses and Authorized Laboratories Has Been Repealed
About the Announcement
According to the announcement published on the official website of the General Directorate of Public Health of the Ministry of Health, the “Instruction on Biocidal Product Analyses and Authorized Laboratories” has been repealed.
Within this scope, the following new documents have been published:
- Instruction on Evaluation of Biological Efficacy Laboratories for Product Types 14, 18, and 19,
- Guideline for the Evaluation of Microbiological/Biological Analyses,
- Guideline for Physical, Chemical, and Stability Tests of Biocidal Products.
This amendment aims to streamline the analysis processes of biocidal products and to enhance the specialization of laboratory units providing analytical services. Therefore, this development is highly relevant to authorized laboratories, institutions offering analytical services within biocidal product authorization processes, and manufacturers and importers of biocidal products.
Companies are required to comply with the new arrangements introduced for biocidal product analyses.
At Chemleg, we closely monitor regulatory developments in the sector and promptly share updates regarding all legislative changes on biocidal products in Türkiye.
For further information, please contact us.