biyo SEARCH
1
                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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2
                OFFICIAL LETTER ON LICENSING BUSINESS AND TRANSACTIONS AND USE OF AUXILIARY ACTIVE SUBSTANCES HAS BEEN PUBLISHED!
22-03-2022
                            The Environmental Health Department has issued the Official Letter dated 10/03/2022 and numbered E-19020089-819-1014, in which it specifies the details of the Biocidal Product licensing work and pr
                            
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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
                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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6
                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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7
                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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8
                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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9
                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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10
                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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11
                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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12
                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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13
                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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14
                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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15
                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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16
                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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