Why TR CLP Labelling Matters
Companies that manufacture or import hazardous chemicals in Türkiye must ensure their labels are fully compliant with the Turkish CLP (Classification, Labelling and Packaging) Regulation, which aligns with the UN’s Globally Harmonized System (GHS). Proper hazard communication is not just a legal obligation but a critical component of workplace and environmental safety.
Correct labelling provides significant benefits. It allows end-users to quickly understand the hazards associated with a product, enabling them to take the necessary precautions and prevent accidents. Beyond hazard pictograms, labels communicate essential information such as product identifiers, hazard and precautionary statements, and supplier details – all of which are vital for emergency responders, healthcare professionals, and firefighters.
Furthermore, non-compliant products cannot be placed on the Turkish market, making accurate labelling essential for both regulatory compliance and market access. Labels also convey environmental risks, guiding users on proper handling and disposal.
What Information Must Be Included on a TR CLP Label?
According to Article 19 of the TR CLP Regulation (often referred to as the SEA Regulation), labels for substances and mixtures classified as hazardous must include:
- Supplier Information: Name, address, and phone number of the responsible party in Türkiye
- Nominal Quantity : The amount of the substance or mixture in the package, unless indicated elsewhere on the packaging (for products placed on the general market)
- Substance or Mixture Identification As specified in Article 20
- Hazard Pictograms: In line with Article 21
- Signal Word: As required under Article 22 (“Danger” or “Warning”)
- Hazard Statements (H-statements): As required under Article 23
- Precautionary Statements (P-statements): As required under Article 24
- Additional Information Section:v As required under Article 27
All labels must be prepared in Turkish. Multilingual labels are acceptable, provided that the Turkish content is complete and identical to all other languages.
Chemleg’s TR CLP Labelling Services
Our expert team supports you throughout the entire labelling process, ensuring technical accuracy and full compliance:
- Hazard Classification: Accurate classification to prevent regulatory non-compliance
- Label Design & Layout: Professional, compliant, and user-friendly designs
- Multi-Language Labelling: Ensure Turkish compliance while supporting international distribution
- Integration with UFI & PCN: Seamless inclusion of UFI codes and alignment with poison centre notifications
- Regulatory Review: Detailed checks to ensure your labels meet SEA requirements before market release
- Ongoing Compliance Updates: Keeping your labels current with regulatory changes
Incorrect labelling can result in fines, product recalls, or market restrictions. Chemleg ensures your chemical labels meet all legal requirements and support safe market access.
Fill out the form now to schedule a consultation with our experts.
Frequently Asked Questions
What are the risks of incorrect TR CLP labelling?
The risks extend beyond legal consequences. Incorrect labelling can lead to serious safety incidents, such as user exposure to toxic substances, improper storage causing fires, or environmental damage due to wrong disposal. Ultimately, non-compliance may result in financial penalties, product recalls, and legal liability.
Does the label have to be in Turkish?
Yes. All labels under the TR CLP Regulation must be in Turkish. Multilingual labels are acceptable, provided that the Turkish content is complete and identical to other languages.
Who is responsible for preparing TR CLP labels?
The responsibility lies with the company placing the product on the market. To ensure compliance, it is highly recommended that labels be prepared or reviewed by expert consultants with in-depth regulatory knowledge. Firms like Chemleg specialise in this service.
How often should labels be reviewed and updated?
Labels must be reviewed whenever there is a change in the formulation or hazard classification of the product, and whenever the TR CLP Regulation is updated. As best practice, regulatory changes should be monitored regularly to ensure ongoing compliance.
