2025-09-09 Reference source : European Commission (EC)
Chemical notification/ registration CLP ECHA update CLP Regulation Update CL Inventory Notifier Details
From
1 July 2026, the European Chemicals Agency (ECHA) will begin publishing the
names of companies that have submitted classification and labelling (C&L)
notifications under the CLP Regulation. The name of every notifier will be made
publicly available in the C&L Inventory in accordance with the amended
Article 42 of the CLP, introduced by Regulation (EU)
2024/2865 published in the EU
Official Journal on 20 November 2024.
Confidentiality Requests
Before June 2026
Companies
wishing to keep their name confidential must update their dossiers and submit a
justification by 30 June 2026. Unless confidentiality is granted, ECHA will make
notifier names publicly accessible from 1 July 2026. ECHA also released an
updated CLP
notification manual in June 2025 to guide
companies through the process.
CLP
Notification Requirements
Manufacturers
and importers placing hazardous substances on the EU market are required to
notify ECHA within a month of placing the substance on the market. Article 40
(1) of the CLP (Classification, Labelling and Packaging) Regulation outlines
the data that must be included in the Substance dataset. The following details
are needed for CLP notification (relevant IUCLID section in brackets):
· Notifier details: Name and contact information (from
REACH-IT).
· Confidentiality request (notifier name): Justification and category must be provided.
· Notifier contact person: To be specified in section 1.1.
· Substance identity: According to Annex VI sections 2.1–2.3.4
(sections 1.1, 1.2, 1.4).
· Confidentiality request (IUPAC name): Provide a publishable name for the C&L
inventory and justification.
· Classification: As required under the CLP Regulation
(section 2.1).
· No classification justification: Required if the substance is not
classified under all hazard classes.
· Reason for classification: Based on supporting data.
· Concentration limits, M-factors, acute
toxicity estimates:
Where applicable, with justification referencing Annex I (section 13).
· Label elements: Hazard pictograms, signal words, hazard
statements.
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