ATTENTION BIOCIDAL PRODUCT MANUFACTURERS AND IMPORTERS!
Content addition date : 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.” In accordance with the provision, the file content of the product must be prepared in accordance with the document titled "Biocidal Product License Application Checklist" and sent to our Ministry physically and electronically.
While applying, application documents must be prepared according to the Biocidal Product License Application Check List as shown in the flow chart below.
Click to view the announcement.
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Download the “Biocidal Product Registration Application Checklist” file. |
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Create a new folder for your product application. Type the name of your product in the name of the folder. |
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Create 4 subfolders in the folder you created. |
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A- Analysis Reports |
B- Administrative Documents |
C- File Contents |
D- Fees and receipts |
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The document name you will upload into the folder must be compatible with the checklist. For example; · A-1- Physical and chemical analysis results · A-2- Accelerated stability test results |
The document name you will upload into the folder must be compatible with the checklist. For example; · B-1- If contract manufacturing, contract manufacturing agreement · B-2- Copy of business and work permit |
The document name you will upload into the folder must be compatible with the checklist. For example; · C-1- Approved formulation document · C-2- Label of the product |
The document name you will upload into the folder must be compatible with the checklist. For example; · D-1- Completeness Fee · D-2- License Evaluation Fee |
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The prepared file must be sent digitally (CD, USB, etc.) and physically. |
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info@crad.com.tr
41° 00' 39" N
29° 06' 14" E
