SEARCH

biocidal SEARCH


1

Is it Acceptable to Submit Copies of Documents Related to the Active Substance?

14-08-2024
Unfortunately, the Authority does not consider copies of documents acceptable. Documents related to the active substance (CoA, report, certificate, etc.) must be obtained from the supplier with a w
continue
2

Our Active Substance Supplier does not want to share the Annex II-A File Requirements due to Confidentiality Reasons, what should we do?

14-08-2024
The Annex II-A active substance data set contains comprehensive information and data about the active substance. The majority of this information is classified as confidential information.
continue
3

How should the Documents be Prepared According to the Biocidal Product License Application Checklist?

14-08-2024
The file must be prepared in accordance with the Checklist and submitted to the Authority. All documents must be prepared with wet signatures. Since the Environmental Health Department does not hav
continue
4

Is Active Substance Registration done in Turkey?

15-03-2024
No, active substance registration is not made within the scope of TR-BPR. Instead, the Annex II-A active substance file, which is the TR-BPR annex, is submitted to the Authority. This file contains
continue
5

Treated Articles or Biocidal Products?

15-03-2024
In this regard, an evaluation should be made on a product basis. The product's claims, content and intended use are important. In order for a correct evaluation to be made, you can contact our
continue
6

In which Laboratory are Biocidal Product Analyzes Performed?

15-03-2024
With the Regulation on Amendments to the Biocidal Products Regulation published in the Official Gazette dated 30/12/2021 and numbered 31705, the definition of authorized laboratory is only valid fo
continue
7

How long does the Biocidal Product Licensing Process take?

15-03-2024
There is no clear time for this. The data provided by manufacturers/applicants and the scope of this data better determine the process. In addition, since the process progresses in line with the de
continue
8

What are our services within the scope of the Biocidal Products Regulation?

15-03-2024
•    Regulatory compliance support and consultancy •    Acting as representative/registrant •    Label compliance in accord
continue
9

What should be done for products falling within the scope of the Biocidal Product Regulation?

15-03-2024
If you offer or want to offer your product to the domestic market with a claim stating that it is a biocidal product, a license application must be made within the scope of TR-BPR. O
continue
10

What Regulations are Followed in the Biocidal Product Registration Process?

15-03-2024
Biocidal Products Regulation (Official Gazette No. 27449 and Dated 31 December 2009) Regulation on Classification, Labelling and Packaging of the Substances and Mixtures (dated 1
continue
11

What is Biocidal Product?

15-03-2024
These are active substances and preparations that contain one or more active substances, are offered for sale in ready-to-use form and have a controlling effect on any harmful organism chemically o
continue
12

2024 BIOCIDAL PRICE TARIFF AND ANALYSIS INFORMATION GUIDE IS PUBLISHED!

01-02-2024
A guide to current price tariffs including all fees requested by the Ministry dur
continue
13

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
continue
14

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
continue
15

IN-SITU GENERATION SYSTEMS INSTRUCTION HAS BEEN PUBLISHED!

02-02-2022
The Turkish Competent Authority has prepared and published the “In
continue
16

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
continue
17

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
continue
18

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
continue
19

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
continue
20

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
continue
21

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
continue
22

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
continue
23

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
continue
24

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
continue
25

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
continue
26

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

04-02-2021
Instructions on Biocidal Product Analysis and Authorised Laboratories wh
continue
27

TURKISH BIOCIDAL PRODUCT REGISTRATION OFFICIAL FEES UPDATED!

26-01-2021
Turkish Biocidal Product Registration official fees were updated in the Guide Bo
continue
28

DETAILS REGARDING THE AMENDMENT TO TURKISH BPR

17-03-2020
Turkish Republic Ministry of Health has published Regulation Amendin
continue
29

REGULATION AMENDING THE TURKISH BIOCIDAL PRODUCTS REGULATION IS PUBLISHED!

17-03-2020
Turkish Republic Ministry of Health has published Regulation Amendin
continue
30

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
continue
31

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
continue
32

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
continue
33

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
continue
34

THSK PUBLISHED A GUIDANCE ON OFFICIAL FEES - 2016

12-01-2016
Turkish Public Health Organization (THSK) published a guidance including curre
continue
35

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
continue
36

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
continue
37

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
continue
38

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
continue
39

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
continue
40

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
continue
41

CRAD SEPTEMBER 2015 NEWSLETTER

17-08-2015
CRAD WILL BE ATTENDING ECHA BIOCIDES STAKEHOLDERS' DAYThe European Chemicals Agency organises its third Biocides Stakeholders' Day on Tuesday 1 September 2015 in Helsi
continue
42

CRAD WILL BE ATTENDING ECHA BIOCIDES STAKEHOLDERS' DAY

17-08-2015
The European Chemicals Agency organises its third Biocides Stakeholders' Day on Tuesday 1
continue
43

10-11 DECEMBER 2014 BIOCIDES-17th ANNUAL CONFERENCE

04-09-2014
The event organised by Chemical Watch under the European Biocides
continue
44

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
continue
45

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
continue
46

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
continue
47

Biocidal Products Regulation No 354/2013

25-12-2013

continue
48

Biocidal Products Regulation No 528/2012

25-12-2013

continue
49

THE POSITION OF ANTIFOULING PAINTS AS A BIOCIDAL PRODUCT

13-09-2013
Boyaturk Magazine - 2013 August-September Antifouli
continue
50

THE POSITION OF ANTIFOULING PAINTS AS A BIOCIDAL PRODUCT

13-09-2013
Boyaturk Magazine - 2013 August-September Antifouli
continue
51

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

26-08-2013
Turkchem Magazi
continue
52

RECENT DEVELOPMENTS IN TERMS OF TURKISH CHEMICAL LEGISLATION WITHIN THE FRAMEWORK OF THE EU ACCESSION NEGOTIATIONS

26-08-2013
Boyatürk Magazine - 2011 August-SeptemberAlthough
continue
53

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
continue
54

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
continue
55

RECENT DEVELOPMENTS IN TERMS OF TURKISH CHEMICAL LEGISLATION WITHIN THE FRAMEWORK OF THE EU ACCESSION NEGOTIATIONS

27-11-2012
Boyatürk Magazine - 2011 August-SeptemberAlthough
continue
56

TURKEY IMPLEMENTS MEASURES ON SDSs, CLP AND BIOCIDES

27-11-2012
Chemical Watch - 2010 December / January 
continue
57

Biocidal Products Directive

10-01-2014

continue
58

BIOCIDAL INDUSTRY

02-06-2012
Biocides which are very commonly used in daily life represent a wide range of products e.g. disinfectants, wood preservatives, rodenticides, antifouling agents (on boats), in-can preservatives, use
continue
59

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
continue
60

TRAINING REGULATIONS OF TURKEY

11-10-2012
While the ultimate form that Global development and industrialization reached today providing people comfortable and practical lives with the support of the state-of-the-art technology, brings als
continue
61

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 Offi
continue
62

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 Offi
continue

CONTACT INFORMATION