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Public activities coordination tool

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).
  • Regulatory management option analysis (RMOA).
  • Regulatory risk management – harmonised classification and labelling (CLH) , SVHC identification, restriction.

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

Tetraphenyl m-phenylene bis(phosphate)

EC / List no: 260-830-6 CAS no: 57583-54-7
Data generation and assessment
DEv - Dossier evaluation
DEv 1
Scope
Comprehensive
Status
Follow-up
Decision date
11/05/2017
Decision
Latest update
23/05/2019
More information View
DEv 2
Scope
Targeted
Status
Follow-up
Decision date
27/04/2018
Decision
Latest update
12/11/2018
More information View
DEv 3
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
13/10/2018
More information View
DEv 4
Scope
Targeted
Status
Concluded
Decision date
09/10/2013
Decision
Latest update
04/10/2018
More information View
DEv 5
Scope
Targeted
Status
Concluded
Decision date
16/08/2013
Decision
Latest update
04/10/2018
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 Reprotoxic
Potential endocrine disruptor
Suspected PBT/vPvB
Consumer use
Exposure of environment
Exposure of workers
High (aggregated) tonnage
Wide dispersive use
Year
2020
Status
Not started
Conclusion document
Latest update
19/03/2019
More information View
ED - Endocrine disruptor assessment
ED 1
Authority
France
Status
Under development under SEV
Outcome
Under development under SEV
Follow-up
No suggestion yet
Hazard assessment outcome document
Remarks
Concern
Endocrine disruption
Date of intention
15/09/2016
Date of hazard assessment
Latest update
13/10/2016
More information View
Regulatory Management Option Analysis
RMOA 1
Authority
France
Concern
Endocrine disruption
Status
Concluded
Outcome
Appropriate to initiate regulatory risk management action
Follow-up
Other
RMOA conclusion document
Remarks
Planned Substance Evaluation 2019 by France
Date of intention
08/02/2016
Date of RMOA conclusion
10/08/2018
Latest update
10/08/2018
More information View

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