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Companies that manufacture or import 1 tonne or more of a substance per year in Turkey (on its own or in a mixture) are subject to registration. Foreign manufacturers can delegate this obligation by appointing an Only Representative.
31 December 2026 for substances of 1,000 t/year and above and high-hazard substances; 2028 for 100–1,000 t/year; 2030 for 1–100 t/year. For interim registration, the deadlines are 31 March 2026 for lead registrants and 30 September 2026 for member/individual registrants.
It is an interim mechanism that allows companies that have made a pre-MBDF notification to keep their substances on the market before full registration; failing to complete interim registration within the deadline puts market access at risk.
No; a separate KKDİK registration is required for Turkey. However, the studies in your REACH dossier can largely be reused in the KKDİK registration.
The Substance Information Exchange Forum; a mandatory platform where companies registering the same substance come together for data sharing and joint submission.
It consists of the Ministry's registration fee (based on tonnage and SME status), Letter of Access (LoA) costs, and consultancy/dossier preparation fees.
A registration obligation may arise if there is intended release of a substance from the article and the substance exceeds 1 tonne per year per article; a notification obligation may arise if the SVHC content exceeds 0.1%.
SEA is Turkey's adaptation of the EU CLP Regulation; the classification system is parallel, but notification authorities, the language requirement and some lists differ.
It is not; calculation methods based on component data and bridging principles can be used. Testing may be required for some physical hazards.
Product identifiers, supplier information, pictograms, signal word, H and P statements, and minimum label dimensions appropriate to the package volume.
The notification of hazardous mixtures to the National Poison Advice Centre for rapid response in poisoning incidents; it is the responsibility of the manufacturer/importer placing the product on the market.
Only preparers certified under the relevant regulation. The Regumind team consists of certified experts.
Turkish is mandatory for the Turkish market. For export markets, a separate SDS is prepared in accordance with the target country's language and regulatory format.
Without delay upon new data affecting classification, an authorization/restriction decision, or a format change; the new version must be sent to recipients from the last 12 months.
An extended form created by attaching exposure scenarios to the SDS for substances subject to a chemical safety assessment.
A substance of very high concern: it creates additional obligations such as supply-chain communication, notification for articles, and the possibility of future authorization requirements.
An Only Representative takes on the registration obligation of the foreign manufacturer; a Third-Party Representative represents you in MBDF/data sharing while keeping the registration under your name and your identity hidden.
No; placing an unauthorized biocidal product on the market is prohibited and subject to administrative sanctions.
Yes; a Cosmetic Product Safety Report (CPSR) must be prepared by a competent safety assessor for every cosmetic product before it is placed on the market.
We conduct a status assessment through a free initial meeting and present a written proposal that clarifies scope and timeline; after approval, we begin work with a project plan.
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