Biocidal Products
Scope of the Legislation:
It determines the procedures and principles regarding the production and importation of biocidal products, their licensing and registration, placing on the market, packaging, labeling, classification, inspection and other issues related to biocidal products in a way that can assess the risks related to human, animal and environmental health before they are placed on the market. Apart from this, it involves real and legal persons who are active in the production, importation and placing on the market of the products and active substances of these products specified in Annex-V (Biocidal Product Types and Their Definitions (Except Product type 1 and 19) or who have been licensed. Inventory records, registration and license certificates are issued for products in accordance with the legislation.
Basic Security Requirements:
In order to obtain inventory records, registration and license certificate, the matters specified in the Legislation must be complied with.
Conformity Mark Required by the Legislation:
Not available.
Conformity Assessment Procedure Required by the Legislation: It is checked whether the application file is complete in accordance with the provisions of this
By-law. In case the file is incomplete, the applicant is notified of the deficiencies in writing and a reasonable time is given according to the nature of the deficiency. If
the deficiency is not corrected after the expiry date, the application will be rejected. Files that are found to be complete as a result of the evaluation are evaluated.
Inventory records, registration and license certificates are issued for products in accordance with the legislation.
Date of Entry Into Force: 31st December 2009/27449 (4th reiterated)
COMMUNIQUE ON BIOCIDAL PRODUCTS WITHOUT ACTIVE SUBSTANCE
Scope of the Legislation:
This Communique; It covers all substances, preparations, articles used for biocidal purposes in the field of public health but not covered by the By-Law on Biocidal Products and their manufacturers and importers.
Basic Security Requirements:
In order to issue the Notification Registration Document for Biocidal Products WithoutNot Containing Active Substances, the matters specified in the Communique must be complied with.
Conformity Mark Required by the Legislation:
Not available.
Conformity Assessment Procedure Required by the Legislation:
Manufacturers or importers have to prepare and report the institution on the notification form in Annex-1 and the label samples of each product type in electronic
environment before the product is placed on the market. A notification is made by issuing the registration document by the institution. A copy of the notification form
is retained by the manufacturer. Manufacturers who make a notification are given a registration number by issuing a Notification Registration Document for Biocidal
Products Not Containing Active Substances by the institution.
Date of Entry Into Force: 2nd August 2013/28736
COMMUNIQUE ON BIOCIDAL TREATED ARTICLES
Scope of the Legislation:
This Communique; It includes substances, mixtures or articles claimed to have biocidal properties or biocidal functions, which are treated with one or more biocidal
products, or which deliberately contain one or more biocidal products.
Basic Security Requirements:
In order to prepare a technical file within the scope of Articles Treated with Biocidal Product, the provisions of the Communique on Biocidal Treated Articles must be complied with.
Conformity Mark Required by the Legislation:
Not available.
Conformity Assessment Procedure Required by the Legislation:
Manufacturers or importers, with regard to the processed goods to be placed on the market; It prepares a technical file containing the analysis reports prepared in
accordance with the provisions of Article 6 titled Classification, Labeling and Packaging, Article 9 titled Technical File and Article 11 titled Analysis, and upon request
by the Ministry within the scope of market surveillance and inspection activities, or inspectors assigned by the Ministry. If requested during the audit, they submit the
technical file and/or other information and documents to the Ministry or the auditor.
Date of Entry Into Force:13th May 2018/30420