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KKDIK (KKDIK) 2026 Risk Analysis
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Official full text of the regulation: KKDIK Regulation - Official Gazette.
What does KKDIK risk analysis measure?
KKDIK risk analysis digitizes your company's vulnerabilities against chemical regulations. For each item in the inventory, role, tonnage, registration status and lack of documentation are evaluated. The aim is to foresee which topic you will have difficulty with when the audit comes.
What topics does the analysis cover?
The scope is grouped under five headings: correct determination of the company role, completeness of the substance inventory, accuracy of tonnage calculation, registration and pre-registration status, set of documents (safety data sheet, label, evidence file). Each title is rated according to its risk level.
The most common findings in the analysis
- Inventory incompatibility with customs data and hidden tonnage
- Failure to take into account substances in the mixture
- Unsubstantiated exemption assumptions based on supplier declaration
- Classification difference between safety data sheet and label
- No downstream user scenario verification has been performed
How do we proceed?
First we get the item list and annual quantities. Then we mark the role and obligation for each line. Then we list the missing documents and the required steps in order of priority. The output is not a technical report; It is an action plan that shows who will do what and when.
Why should it be done early?
As the deadline approaches, forums get busier, data access fees get higher, and lab lines get longer. Risk analysis shows which items are truly critical before this cost increase. Thus, the budget is allocated to the riskiest items.
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How are risk levels determined?
We use three levels for each item. High risk are substances that exceed the threshold and are not registered; these carry the risk of a market ban. Medium risk are substances that are registered but lack documentation; It causes non-compliance in the audit. Low risk are substances that are below the threshold and are sufficient to be monitored.
What do we deliver in the report?
The report consists of two parts. The first section is the item-by-item table: role, tonnage, registration status, missing documentation and risk level. The second part is the action plan: which steps should be done, in what order, by which date. Thus, the report turns from a list of determinations into an actionable calendar.
Who is it suitable for?
It is suitable for any company that produces, imports or formulates mixtures of chemicals. Especially in companies that purchase from many suppliers and have dispersed inventories, analysis reveals hidden liabilities.