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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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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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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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