Experto CLP Regulation (Classification, Labelling and Packaging)

The CLP Regulation (Classification, Labelling and Packaging) is a cornerstone of chemical safety in Europe. Understanding its requirements is essential for professionals involved in regulatory affairs, product stewardship, EHS, quality, manufacturing, purchasing, logistics, and supply chain management.

Whether you are new to chemical regulations or looking to strengthen your expertise, this course will provide the knowledge and practical skills needed to navigate CLP requirements confidently and ensure compliance within your organization.

A key advantage of this course is the participation of external experts from leading organizations such as FEIQUE and Kerona Scientific, who bring extensive experience in chemical regulation and industry compliance.

Their contribution will provide valuable insights into current regulatory challenges, real-world case studies from the chemical industry, best practices for implementing CLP requirements and engaging discussions with experienced professionals from the sector.

Provide a comprehensive understanding of the CLP Regulation and its role within the European chemical’s legislation framework.
Explain the principles of hazard classification for physical, health, and environmental hazards.
Understand the legal obligations of manufacturers, importers, downstream users, and distributors.
Learn how to correctly classify substances and mixtures according to CLP criteria.
Develop the ability to interpret and apply hazard pictograms, signal words, hazard statements (H-statements), and precautionary statements (P-statements).
Understand the requirements for the labelling and packaging of chemical products.
Learn how CLP interacts with REACH, Safety Data Sheets (SDS), and other regulatory requirements.
Promote safe handling and communication of chemical hazards across the supply chain.
Support regulatory compliance and reduce the risks associated with chemical use and distribution.

Topic 1. Understanding the general objectives of the CLP Regulation, its scope of application, and amendments.
Topic 2. Identifying the appropriate labelling for each mixture.
Topic 3. Applying the appropriate hazard communication tool in each case.
Topic 4. Understanding hazard pictograms, signal words, and hazard statements.
Topic 5. Translating the classification of Directive 67/548/EEC into the CLP classification.
Topic 6. Applying classification criteria using real-life examples.
Topic 7. European Ecolabel.
Topic 8. What endocrine disruptors are and how they act.
Topic 9. Categorisation of endocrine disruptors (EDs): endocrine disruption for human health and endocrine disruption for the environment.
Topic 10. Identification of endocrine disruptors: in vitro and in vivo evaluation protocols (aquatic environment) and mammals.
Topic 11. Endocrine disruptors and their inclusion in the CLP Regulation.
TEAMS session
Practical case study
Final examination