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Updated ECHA Q&A document on the restriction of Cr(VI) substances is available

Of particular interest is the question of what impact the entry into force of the restriction will have on existing authorizations. As things stand at present, the restrictions are set to come into force in 2027, with existing authorizations losing their validity after 18 months at the latest. Authorization applications that have already been submitted would receive a correspondingly shorter authorization period.

Against this background, ECHA will give priority to applications for authorization of other substances over authorization applications and review reports for Cr(VI) substances in the period before the restriction comes into force. Furthermore, applications for authorization from new users will take priority over review reports for Cr(VI) substances. It is therefore unlikely that the process will be completed before the restriction comes into force, particularly for the submission of review reports.

In view of the emerging developments, it is all the more important that the industry takes advantage of the opportunity to comment on the Annex XV dossier prepared by ECHA and addresses the emerging issues. This must be done by September 18, 2025. Comment on ECHA website

Download the recent Q&A document via CIRCABC: European Commission updates Q&As on Chromium(VI) compounds

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Classification of titanium dioxide revoked

The European Court of Justice (EuGH) has revoked the classification of titanium dioxide (TiO2). Since 2021, TiO2 powder containing particles with an aerodynamic diameter of ≤ 10 μm had to be classified as “probably carcinogenic when inhaled” (Carc. 2) and labelled accordingly.

Shortly after the classification decision was made, the industry spoke out against this classification, as TiO2 is indispensable as a colour pigment. In 2022, a lawsuit was filed with the EuGH against the classification, and an appeal was lodged against an initial ruling.

In August, the ruling that the classification of TiO2 should be revoked was confirmed. The classification was based on flawed studies. The next step is to repeal the 14th ATP by means of an implementing regulation.

The judgment can be viewed here: https://curia.europa.eu/jcms/upload/docs/application/pdf/2025-08/cp250099de.pdf

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New REACH Enforce project (REF-15) introduced

In 2027, inspections will be carried out in companies that

  • handle substances of very high concern (SVHC)
  • have a valid authorization for Annex XIV substances.

The aim is to check restrictions on use in accordance with Annex XIV (authorization) and Annex XVII (restriction), REACH. The inspections are carried out by the national/municipal authorities. These are announced in advance.

The REF project aims to improve worker safety and strengthen enforcement by improving cooperation between the enforcement authorities responsible for REACH and the authorities responsible for occupational health and safety regulations. The evaluation is expected in 2028.

ECHA Enforcement Forum: https://echa.europa.eu/about-us/who-we-are/enforcement-forum

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