Will the CLP revision achieve its goal of making the obligations of market players more pragmatic and legally secure?
Together with the REACH Regulation and POP Regulation, the CLP Regulation forms the core of chemicals’ regulation in the EU. The CLP Regulation regulates the classification, labelling and packaging of chemical substances. Following its publication in the Official Journal on 20 November 2024, the revised CLP Regulation will enter into force on 10 December 2024.
Backgrounds
The Commission considered that adjustments to the regulation were necessary to keep pace with technological and scientific developments. In addition to the adoption of new hazard classes that have already been introduced and adjustments to classification, the revisions of the labelling and information obligations are particularly relevant.
Revision of the labelling requirements
The previous regulations on labelling obligations revealed considerable room for interpretation and caused legal uncertainty among market players. Not least because of the numerous feedback from affected companies, central regulations have been substantiated.
- Formatting: the minimum requirements for labelling (e.g. font size, spacing or colour) have been revised and substantiated.
- Folding labels: until now, the use of folding labels was only permitted in justified exceptional cases, whereby the prerequisites for these exceptions were partly unclear, or at least impractical. Folding labels may in the future be used as an equivalent alternative, subject to special design requirements.
- Digital labelling: the CLP revision defines the framework conditions for digital labelling. However, physical labelling is still required, digital labelling can or may only be provided in addition (except for supplementary information).
- Online trading: In the future, labelling elements must also be indicated for so-called distance selling transactions (especially in online trading). In this respect, the CLP Regulation substantiates the requirements of Article 31 of Regulation (EU) 2022/2065 (‘Digital Services Act’).
Information obligations
- Powers of the ECHA: Information on emergency healthcare must be transmitted to notified bodies (poison control centres) at national level. The CLP Regulation only provides that this task can be taken over centrally and throughout Europe by ECHA; however, only if an EU member state delegates these powers to ECHA.
- Obligations of market players: Amendments to Article 45 of the CLP Regulation clarify that importers, downstream users and distributors may also be obliged to submit information to notified bodies in accordance with Annex VIII Part B of the CLP Regulation (which has also been extended).
Conclusion
It remains to be seen whether the CLP revision will make the legal framework for substances and mixtures more legally secure and pragmatic. In particular, the potential for a practical design of labelling and information obligations through digitalisation and standardisation has not been exploited.
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