Turkey's KKDIK End-of -2023 Deadline Approaching, Lead Registration Slow

Release time:

2023-09-05 14:42

After January 1, 2024, Turkish overseas suppliers or Turkish importers must complete the official registration of all substances produced or imported in Turkey with an annual production of ≥ 1 ton before they can export or import. Manufacturers outside Turkey must fulfill their registration obligations through a single representative (OR) in Turkey, and the relevant registration files need to be submitted through the KKS system

For substances for which there is currently no leading registrant LR, Chinese enterprises can entrust OR in Turkey (New Anrun Consulting will provide one-stop service) to act as LR and complete the registration as soon as possible. For substances that already have LR, the cost of the leading registration project for some substances has been clarified, and the project cost for some substances is still under calculation. It is expected to be relatively clear in the fourth quarter of 2023, when Chinese enterprises can purchase data fees to complete the registration. Due to the large number of files to be submitted, overall, the lead registration nomination and lead registration files are submitted slowly, and the data costs for many substances are not yet clear.

Registration numbers are generally available within one month of the submission of the dossier, but as the deadline approaches, the review cycle of the Turkish authorities is expected to be extended.

In order to speed up the registration process, the Turkish Ministry of Environment, Urbanization and Climate Change (MoEUCC) recently issued new implementation guidelines in accordance with the KKDIK Regulation on the Registration of Chemicals in Turkey. Under the new guidelines, it is not mandatory to provide importer information when registering substances. Chemical Safety Reports (CSR) can also be submitted in English, with additional time to submit Turkish translations after the registration deadline. In addition, "Registrant Identity" and "Registration Number" may be classified as Commercial Information Confidential (CBI).

If there is a need for KKDIK registration, contact 15801695345 Manager.

The United States has repeatedly expanded the "entity list" of export controls-the small science of the entity list.

Recent News of the European Chemicals Agency (ECHA)

The United States has repeatedly expanded the "entity list" of export controls-the small science of the entity list.

Recent News of the European Chemicals Agency (ECHA)

Latest developments

Key Illustration of Railway Transportation Regulations for Consumer Lithium Battery Cargo

Recently, the Ministry of Industry and Information Technology of the National Railway Administration China National Railway Group Co., Ltd. announced the guidance on the railway transportation of consumer lithium battery goods. For details, please refer to our public article. Official

Answers to Frequently Asked Questions about the Environmental Management Measures for New Chemical Substances (Order No.7)

I recommend: For pre-registration projects with large tonnage and short grace period, or small tonnage pre-registration projects that are clearly registered in the future, it is recommended to choose joint registration and join the joint registration IT system agreement this time. For pre-registration projects that are clearly not registered in the future, it is recommended to choose subsequent registration. May I ask you

Cancellation of GMP certification means stricter supervision of drug production?

The cumbersome process of GMP and GSP certification has made many pharmaceutical manufacturers and distribution companies feel the strict supervision of the pharmaceutical industry. On September 25, 2019, the State Food and Drug Administration issued a notice on the study, publicity and implementation of the the People's Republic of China Drug Administration Law., It is clearly proposed to strengthen dynamic supervision and cancel the drug production quality management practice (GMP) certification and the drug business quality management practice (GSP) certification.