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biocidal product regulation in turkey SEARCH


1

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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2

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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3

Where the Biocidal Product Analysis should be Performed?

29-01-2019
After the Provisional Application approval, which is the initial stage of the full Registration Process, the analysis should be performed at the Authorised Turkish Laboratories with the samples tha
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4

What are the Official Fees Demanded by Ministry through the Biocidal Product Registration Process?

29-01-2019
 
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5

How can I check the status of an active substance?

24-05-2018
The Active substance lists published on the official website of the Turkish Ministry of Health.  •    List A :
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6

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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7

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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8

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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9

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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10

CRAD DECEMBER 2015 NEWSLETTER

07-12-2015
THSK HAD PUBLISHED A DECLARATION ON THE VIRUS EFFICACY TEST UNDER THE SCOPE OF TR - BPR In order to register biocidal products under the scope of Biocidal Products Reg
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11

THSK HAD PUBLISHED A DECLARATION ON THE VIRUS EFFICACY TEST UNDER THE SCOPE OF TR - BPR

07-12-2015
In order to register biocidal products under the scope of Biocidal Products Re
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12

THSK HAD PUBLISHED A DECLARATION ON THE VIRUS EFFICACY TEST UNDER THE SCOPE OF TR - BPR

07-12-2015
In order to register biocidal products under the scope of Biocidal Products Re
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13

CRAD MARCH 2014 NEWSLETTER

27-03-2014
CORRIGENDUM TO TURKISH BIOCIDAL PRODUCTS REGULATION IS PUBLISHEDCorrigendum to Turkish Biocidal Product Regulation is published on 12 March 2014 dated on the Official Gazette
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14

CORRIGENDUM TO TURKISH BIOCIDAL PRODUCTS REGULATION IS PUBLISHED

12-03-2014
Corrigendum to Turkish Biocidal Product Regulation is published on 12 March 2014 dated on the Official Gazette with No: 28939 and came into force on the date of publication. Som
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15

Biocidal Product Regulation Compliance, Registration & Consulting Services

11-10-2012
Registration of Biocidal Products under the scope of Biocidal Products Regulation (OG, 27449, 31.12.2009) Biocidal Products Regulation has been published in the Official
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16

Biocidal Product Regulation Compliance, Registration & Consulting Services

11-10-2012
Registration of Biocidal Products under the scope of Biocidal Products Regulation (OG, 27449, 31.12.2009) Biocidal Products Regulation has been published in the Official
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