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1

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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2

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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3

DETAILS REGARDING THE AMENDMENT TO TURKISH BPR

17-03-2020
Turkish Republic Ministry of Health has published Regulation Amendin
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4

REGULATION AMENDING THE TURKISH BIOCIDAL PRODUCTS REGULATION IS PUBLISHED!

17-03-2020
Turkish Republic Ministry of Health has published Regulation Amendin
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5

What is the Biocidal Product Regulation?

24-05-2018
Biocidal Product Regulation (BPR) has been published in the Official Gazette with No: 27449 on the date 31 December 2009. The Turkish BPR has been prepared in accordance with EU directive 98/8/EC,
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6

What is the definition of a biocidal product under the Turkish BPR?

24-05-2018
Article 3 of the Turkish Biocidal Product Regulation defines a biocidal product as “Active substances and preparations containing one or more active substances, put up in the form in whi
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7

What are CRAD’s services under the scope of Turkish Biocidal Product Regulation?

24-05-2018
Turkish Ministry of Health has implemented the EU BPD 98/8/EC and published the Biocidal Product Regulation in the Official Gazette with No: 27449 on the date 31 December 2009. 
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8

Do I need to apply an approval/authorisation/registration before I sell my biocidal product in Turkey?

24-05-2018
Yes, the Biocidal Products have to be notified or registered according to the Turkish Biocidal Product Regulation in order to be placed on the market. The biocidal products could
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9

THSK PUBLISHED A GUIDANCE ON OFFICIAL FEES - 2016

12-01-2016
Turkish Public Health Organization (THSK) published a guidance including curre
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10

THSK ANNOUNCES A DECLARATION ON REVOKING OF SOME BIOCIDAL PRODUCT LICENCES BASED ON THE COMMISSION DELEGATED REGULATION (EU) NO 1062/2014

17-12-2015
As the 12 month transition term that applies to some of the active substances
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