PACT - Public Activities Coordination Tool

PACT - Public Activities Coordination Tool

PACT - Public Activities Coordination Tool

The public activities coordination tool (PACT) provides an overview of the substance-specific activities that authorities are working on under REACH and the CLP Regulation. These activities are being carried out in line with ECHA’s Integrated Regulatory Strategy.

PACT provides up-to-date information on the activities planned, ongoing or completed by ECHA and/or MSCAs for a given substance in the following areas:

  • Data generation and assessment – dossier evaluation, substance evaluation, informal hazard assessment (PBT/vPvB/ED).
  • Assessment of regulatory needs (ARN).
  • Regulatory risk management – harmonised classification and labelling (CLH) , SVHC identification, recommendations for inclusion in the Authorisation List, restriction.

A summary of all the substance-specific activities can be found under ‘Details’ for each entry.

Octocrilene

EC / List no: 228-250-8 CAS no: 6197-30-4
Data generation and assessment
DEv - Dossier evaluation
DEv 1
Scope
Testing Proposal
Status
Follow-up
Decision date
27-aug-2021
Decision
Latest update
06-dec-2023
Additional information
More information View
SEv - Substance evaluation (Community Rolling Action Plan (CoRAP))
SEv 1
Evaluating Member State
France
Co-Evaluating Member State
Initial grounds for concern
Suspected PBT/vPvB
High (aggregated) tonnage
Wide dispersive use
Year
2012
Status
Information requested
Conclusion document
Latest update
21-jul-2022
More information View
PBT - Persistent, bioaccumulative and toxic assessment
PBT 1
Authority
France
Status
Under development
Outcome
Under development under SEV
Hazard assessment outcome document
Remarks
Concern
PBT (Article 57 d)
Date of intention
03-feb-2012
Date of hazard assessment
Latest update
01-apr-2015
More information View
Regulatory risk management
Restriction
Restriction 1
Status
Intention
Date of intention
04-okt-2023
Withdrawal date
Submitter(s)
France
Remarks
Stakeholders are requested to provide relevant information to the Dossier Submitter. If justified based on robust risk and socio-economic information the Dossier Submitter may propose derogations from the proposed restriction. If a derogation is not proposed by the Dossier Submitter then it will be incumbent on the relevant stakeholders to do so during any consultation process with a full risk and socio-economic justification accompanying it.

Submission date postponed due to internal planning considerations.
Details on the scope of restriction
Restricting the placing on the market of mixtures containing octocrilene.
Restriction report (and annexes)
Opinion of RAC (and minority positions) and Forum Enforceability Advice (as of September 2023)
Draft opinion of SEAC
Compiled RAC and SEAC opinion (and minority positions)
Adopted restriction/Commission communication
Latest update
29-jan-2024
More information View
Assessment of regulatory needs
ARN 1
Authority
France
Concern
Bioaccumulation
Endocrine disruption
Other environmental toxicity
Other human toxicity
Persistence
Toxic for reproduction
Status
Under development
Follow-up
No suggestion yet
Foreseen regulatory need
Summary document
Group name
Remarks
Link to public consultation of the draft RMOA : https://www.consultations-publiques.developpement-durable.gouv.fr/projet-de-rmoa-analyse-de-la-meilleure-option-de-a2895.html
Date of intention
31-jul-2023
Date of assessment
Latest update
01-aug-2023
More information View

List entry date: 14-jan-2016

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