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1

DECISION ON NON-APPROVAL OF ACTIVE SUBSTANCES HAS BEEN PUBLISHED!

11-09-2023

It has been decided that the relevant substances will not be approved for use as biocidal product active ingredients in the specified product types based on COMMISSION IMPLEMENTING DECISION (EU) 20
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2

ATTENTION BIOCIDAL PRODUCT MANUFACTURERS AND IMPORTERS!

04-08-2023

In the first paragraph of Article 11 of the Biocidal Products Regulation, “…. The Ministry may request the content of the file in a physical and/or electronic carrier environment.&rdqu
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3

IN-SITU GENERATION SYSTEMS INSTRUCTION HAS BEEN PUBLISHED!

02-02-2022

The Turkish Competent Authority has prepared and published the “In
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4

ACTIVE SUBSTANCE REGISTRATION SCIENTIFIC COMMITTEE FIRST MEETING HELD

01-12-2021

The Scientific Committee on Active Substance Registration, appointed by the General Directorate of Public Health (HSGM) with the official letter dated 24.11.2021 and numbered E-19020089-020-4826, h
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5

ABOUT CESSATION OF USE OF CERTAIN ACTIVE SUBSTANCES

19-10-2021

The European Commission Implementation Decree dated 02/08/2021 and numbered 2021/1283/EU, published in the Official Journal of the European Union dated 03/08/2021 and numbered L279, entered into fo
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6

THE INSTRUCTIONS ON BIOCIDAL PRODUCT ANALYSIS AND AUTHORIZED LABORATORIES HAVE BEEN UPDATED!

24-09-2021

The Instructions on Biocidal Product Analysis and Authorized Laboratories which were published by the General Directorate of Public Health dated 16/08/2021 and numbered E-19020089-020-3305 have bee
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7

THE INSTRUCTIONS ON BIOCIDAL PRODUCT ANALYSIS AND AUTHORIZED LABORATORIES HAVE BEEN UPDATED!

17-08-2021

The Instructions on Biocidal Product Analysis and Authorized Laboratories which were published by the General Directorate of Public Health dated 29/01/2021 and numbered E-19020089-105.99-99-4 have
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8

THE DRAFT REGULATION ON THE AMENDMENT OF THE BIOCIDAL PRODUCTS REGULATION HAS BEEN ANNOUNCED!

17-08-2021

The Ministry of Health of the Turkish Republic has announced the draft regulation on the Amending of the Biocidal Products Regulation aiming to bring the current Biocidal Products Regulation and it
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9

THE USE OF ESBIOTHRIN AS AN ACTIVE SUBSTANCE IN BIOCIDAL PRODUCTS HAS BEEN SUSPENDED.

16-08-2021

The Commission Implementing Decision (EU) 2021/98 published in the Official Journal of the European Union dated 29/01/2021 and numbered L31, not approving esbiothrin as an existing active substance
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10

BIOCIDAL PRODUCT LICENSE VALIDITY PERIODS HAVE BEEN UPDATED!

02-06-2021

As known, the license validity periods of all biocidal product licenses issued following the provisions of the Biocidal Product Regulation dated 31 December 2009 and 27449 (4th bis.) will expire on
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11

THE INSTRUCTIONS ON BIOCIDAL PRODUCT ANALYSIS AND AUTHORISED LABORATORIES HAS BEEN UPDATED!

04-02-2021

Instructions on Biocidal Product Analysis and Authorised Laboratories wh
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12

MINISTRY OF HEALTH HAS PUBLISHED THE INSTRUCTIONS ON BIOCIDAL PRODUCT ANALYSIS AND AUTHORISED LABORATORIES.

20-02-2019

Working Procedures and Principles of Biocidal Product Analysis Laboratories
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