Our Services

KKDİK Consultancy & Registration Services

We provide comprehensive consultancy on determining your KKDİK obligations for chemical substances in Türkiye and on managing registration and notification processes.

Scope of Service

01

Chemical Regulatory Consultancy

Consultancy is provided on assessing KKDİK obligations concerning the registration, evaluation, authorisation and restriction of chemicals in Türkiye, and on carrying out registration processes.

  • CLP (SEA) NotificationCarrying out notification processes for the classification and labelling of chemicals.
  • SDS PreparationPreparing and updating Safety Data Sheets for chemicals.
  • Chemical Inventory PreparationOrganising a company’s chemical substances and related information into an inventory.
Request a quote for this service
02

KKDİK Pre-Registration

Support is provided in assessing the pre-registration status of chemical substances, preparing the required information and carrying out the related procedures.

Request a quote for this service
03

KKDİK Provisional Registration

Consultancy is provided on assessing the requirements for provisional registration, preparing the registration dossier and coordinating the related application processes.

Request a quote for this service
04

KKDİK Full Registration

Support is provided in assessing the data requirements for the substance, preparing the technical documentation and carrying out the full registration process.

Request a quote for this service
05

KKDİK Lead Registrant Registration

Support is provided in taking on the lead registrant role in joint registration processes, coordinating the registration, sharing data and managing communication with the parties involved.

Request a quote for this service

Frequently Asked Questions

What is KKDİK and which companies does it concern?

KKDİK is the regulation on the registration, evaluation, authorisation and restriction of chemicals in Türkiye. Obligations for substances manufactured or imported in Türkiye are assessed according to the type of substance, annual tonnage, use, exemption status and the timeline in force.

Is it enough that an action has already been taken for an existing substance?

Not always. Whether a pre-registration, a provisional registration or a previously prepared dossier meets the current obligations must be checked separately. The company’s role, substance identity, tonnage and dossier status are reviewed together.

What is the difference between pre-registration, provisional registration and full registration?

They refer to different stages and obligations. Which action is required is determined by assessing the substance’s placing-on-the-market status, the company’s role, tonnage and the applicable provisions. The same path may not apply to every substance.

Who is the lead registrant?

The party that coordinates the dossier in a joint registration process. The appointment and duties of the lead are handled within the relevant legislation and KKS processes. Whether a company becomes the lead is assessed according to the substance and the existing registration group.

What is the MBDF (SIEF), and does my company need to join?

The MBDF (Substance Information Exchange Forum, SIEF) is the forum in which registrants of the same substance coordinate information sharing and joint registration processes. Participation and obligations should be assessed according to the substance’s identity, registration status and the relevant legislation.

Does the KKS being open mean all registration deadlines have been extended?

The KKS (Chemical Registration System) continuing to accept submissions does not in itself mean that all legal deadlines have been extended. For each substance and obligation, the current Ministry announcements and the timeline in force should be used as the basis. In Kİ-Chem’s announcements, dates and scope information should be shared together with the up-to-date source.

What information and documents are needed for registration?

Generally, the substance identity and composition, annual tonnage, areas of use, supply chain information, existing test/data documents and the company’s role under the legislation are assessed. The exact document list is drawn up once the scope of the substance and dossier has been determined.

How long does preparing a registration dossier take?

The duration varies depending on data availability, the clarity of the substance identity, the need for data sharing, tonnage and the complexity of the dossier. After a preliminary review, a work plan and an estimated timeline are shared.

See all questions

+90 216 235 04 20

Let’s find the right regulatory path for your product

Share your product and target market details; we will prepare a quote covering the needs analysis, scope and timeline.