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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.

Tributyl O-acetylcitrate

EC / List no: 201-067-0 CAS no: 77-90-7
Data generation and assessment
DEv - Dossier evaluation
DEv 1
Scope
Comprehensive
Status
Follow-up
Decision date
08/12/2017
Decision
Latest update
24/06/2019
More information View
DEv 2
Scope
Comprehensive
Status
Follow-up
Decision date
24/07/2017
Decision
Latest update
04/02/2019
More information View
DEv 3
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
13/10/2018
More information View
ED - Endocrine disruptor assessment
ED 1
Authority
France
Status
Concluded
Outcome
not ED
Follow-up
None
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
12/11/2014
Date of hazard assessment
15/10/2016
Latest update
19/12/2016
More information View
Regulatory Management Option Analysis
RMOA 1
Authority
France
Concern
Endocrine disruption
Status
Concluded
Outcome
No need to initiate further regulatory risk management action at this time
Follow-up
None
RMOA conclusion document
Remarks
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.
Date of intention
12/11/2014
Date of RMOA conclusion
07/11/2016
Latest update
07/11/2016
More information View

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