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.

Terephthalic acid

EC / List no: 202-830-0 CAS no: 100-21-0
Data generation and assessment
DEv - Dossier evaluation
DEv 1
Scope
Comprehensive
Status
Information requested
Decision date
04-May-2023
Decision
Latest update
05-Jul-2023
Additional information
More information View
DEv 2
Scope
Testing Proposal
Status
Follow-up
Decision date
02-Nov-2021
Decision
Latest update
09-Aug-2023
Additional information
More information View
DEv 3
Scope
Targeted
Status
Concluded
Decision date
29-Jan-2013
Decision
Latest update
26-Nov-2022
Additional information
More information View
ED - Endocrine disruptor assessment
ED 1
Authority
France
Status
Concluded
Outcome
not ED
Hazard assessment outcome document
Remarks
Regarding the outcome of the ED assessment, refer to RMOA conclusion document. Reason for selecting the substance for hazard assessment development: substance known/suspected to be used as an alternative to a SVHC already on the Candidate List.
Concern
Endocrine disruption
Date of intention
05-Sep-2014
Date of hazard assessment
15-Nov-2015
Latest update
11-Dec-2015
More information View
Regulatory risk management
Assessment of regulatory needs
ARN 1
Authority
ECHA
Concern
Status
Under development
Follow-up
CCH
Foreseen regulatory need
Currently no EU RRM action needed
Summary document
Group name
Isophthalates, Terephthalates and Trimellitates
Remarks
Date of intention
05-Mar-2021
Date of assessment
26-Jul-2021
Latest update
08-Dec-2021
More information View
ARN 2
Authority
France
Concern
Endocrine disruption
Status
Concluded
Follow-up
None
Foreseen regulatory need
Summary document
Group name
Remarks
Reason for selecting the substance for RMOA development: substance known/suspected to be used as an alternative to a SVHC already on the Candidate List.
Date of intention
12-Nov-2014
Date of assessment
07-Mar-2017
Latest update
24-Nov-2021
More information View

List entry date: 03-Oct-2018

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