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1

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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2

THE REGULATION ON THE AMENDMENT OF THE BIOCIDAL PRODUCTS REGULATION HAS BEEN COME INTO FORCED!

30-12-2021
The Ministry of Health of the Turkish Republic has published the r
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3

USAGE OF UTS BIOCIDAL MODULE AND EXTENSION OF LICENSE VALIDITY FOR BIOCIDAL PRODUCTS IN DIRECT CONTACT WITH THE HUMAN BODY (PRODUCT TYPE-1 AND PRODUCT TYPE-19)

01-12-2021
With the announcement published by Turkish Medicines and Medical Devices Agency (TİTCK), It has been stated that as of 09.12.2021, registration applications for product type-1 and product type-19 b
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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

LABORATORY INSTRUCTION ON PT-1 AND PT-19 BIOCIDAL PRODUCT ANALYSES HAS BEEN PUBLISHED!

10-03-2021
Product Type-1 and Product Type-19 biocidal products whose duties and responsibilities were transferred to the Turkish Medicines and Medical Devices Agency (TİTCK) has published the laboratory inst
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12

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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13

TURKISH BIOCIDAL PRODUCT REGISTRATION OFFICIAL FEES UPDATED!

26-01-2021
Turkish Biocidal Product Registration official fees were updated in the Guide Bo
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14

DETAILS REGARDING THE AMENDMENT TO TURKISH BPR

17-03-2020
Turkish Republic Ministry of Health has published Regulation Amendin
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15

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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16

DRAFT OF THE REGULATION AMENDING THE TURKISH BIOCIDAL PRODUCTS REGULATION IS PUBLISHED

30-12-2019
Ministry of Health of Turkish Republic published the Draft of the Regulatio
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17

CHANGE OF THE COMPETENT AUTHORITY FOR BIOCIDAL PRODUCTS IN DIRECT CONTACT WITH THE HUMAN BODY (PRODUCT TYPE-1 AND PRODUCT TYPE-19)

13-12-2019
For Biocidal Products which are in direct contact with the human body (eg.Product Type-1 and Product Type-19); the Competent Authority role under the scope of Turkish Biocidal Prod
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18

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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19

What are the Criteria for the Target Microorganism Determination for the Biocidal Products?

29-01-2019
The target microorganisms need to be compliant with the Working Procedures and Principles of Biocidal Product Analysis Laboratories. You may contact with CRAD team for further inf
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20

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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21

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

29-01-2019
 
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22

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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23

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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24

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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25

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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26

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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27

MINISTRY OF HEALTH HAS PUBLISHED THE COMMUNIQUE ON ARTICLES THAT ARE TREATED WITH BIOCIDAL PRODUCTS

15-05-2018
Turkish Ministry of Health (MoH) has published the Communique on Treated Articles (Communique on articles which are treated with Biocidal Products) in the Official Gazette with No: 30420 on the dat
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28

Betül GÜRLEYİCİ DENİZ / Chemist- Biocidal Product Registration Specialist

29-01-2018
Betül Gürleyici was born in İstanbul in 1991. After having her education at General Ali Rıza Ersin High School, she graduated from Depertmant of Chemistry at the University of Yıldız Tekn
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29

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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30

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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31

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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32

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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33

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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34

CRAD OCTOBER 2015 NEWSLETTER

16-10-2015
MINISTRY OF HEALTH HAS PUBLISHED A DRAFT COMMUNIQUE ON TREATED ARTICLEAs well-known Turkey has implemented the BPD as of 2009. However, as that Regulation does not con
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35

MINISTRY OF HEALTH HAS PUBLISHED A DRAFT COMMUNIQUE ON TREATED ARTICLE

01-09-2015
As well-known Turkey has implemented the BPD as of 2009. However, as that Regulation does not contain any definition or details how the treated articles should be regulated, Ministry Of Health is p
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36

10-11 DECEMBER 2014 BIOCIDES-17th ANNUAL CONFERENCE

04-09-2014
The event organised by Chemical Watch under the European Biocides
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37

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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38

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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39

19-22 MARCH 2014 4th NATIONAL BIOCIDAL CONGRESS

10-02-2014
4th National Biocidal Congress, will be held by the cooperation with Yıldırım Beyazıt U
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40

Biocidal Products Regulation No 354/2013

25-12-2013

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41

Biocidal Products Regulation No 528/2012

25-12-2013

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42

What is Biocidal Product?

27-11-2013
Active substances and preparations containing one or more active substances, put up in the form in which they are supplied to the user, intended to destroy, de ter, render harmless, prevent the act
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43

THE POSITION OF ANTIFOULING PAINTS AS A BIOCIDAL PRODUCT

13-09-2013
Boyaturk Magazine - 2013 August-September Antifouli
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44

THE POSITION OF ANTIFOULING PAINTS AS A BIOCIDAL PRODUCT

13-09-2013
Boyaturk Magazine - 2013 August-September Antifouli
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45

THE REGISTRATION PROCESS OF BIOCIDAL PRODUCTS AND CIRCUMSTANCE OF ARTICLES WHICH ARE TREATED WITH THE ACTIVE SUBSTANCE

26-08-2013
Turkchem Magazi
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46

THE REGISTRATION PROCESS OF BIOCIDAL PRODUCTS AND CIRCUMSTANCE OF ARTICLES WHICH ARE TREATED WITH THE ACTIVE SUBSTANCE

12-08-2013
Turkchem Magazine - 2013 July-AugustW
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47

25 JUNE 2013 ECHA BIOCIDES STAKEHOLDER'S DAY

14-06-2013
European Chemicals Agency ( ECHA) is organizing the first Biocidal Stakeholders' Day regarding the implementation of the new Biocidal Product Regulation of the European Union.The Stak
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48

Biocidal Products Directive

10-01-2014

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49

Biocidal Product Directive Training

11-10-2012
Biocidal Products Regulation which has been prepared and ones provisions implemented by MoH, published and came into force on the Official Gazette dated 31 December 2009, numbered 27449 (4. Bis). T
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50

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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51

Biocidal Product Directive Training

11-10-2012
Biocidal Products Regulation which has been prepared and ones provisions implemented by MoH, published and came into force on the Official Gazette dated 31 December 2009, numbered 27449 (4. Bis). T
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52

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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