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.

A mixture of: bis(2,2,6,6-tetramethyl-1-octyloxypiperidin-4-yl)-1,10-decanedioate; 1,8-bis[(2,2,6,6-tetramethyl-4-((2,2,6,6-tetramethyl-1-octyloxypiperidin-4-yl)-decan-1,10-dioyl)piperidin-1-yl)oxy]octane

TINUVIN 123 EC / List no: 406-750-9 CAS no: 129757-67-1
Data generation and assessment
DEv - Dossier evaluation
DEv 1
Scope
Comprehensive
Status
Concluded
Decision date
Decision
Latest update
26-nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision.
More information View
DEv 2
Scope
Testing Proposal
Status
Concluded
Decision date
03-jul-2013
Decision
Latest update
26-nov-2022
Additional information
The draft decision or request was referred to the European Commission for decision-making.
More information View
DEv 3
Scope
Testing Proposal
Status
Concluded
Decision date
Decision
Latest update
26-nov-2022
Additional information
ECHA has stopped the assessment after the registrant(s) submitted new information.
More information View
Regulatory risk management
CLH - Harmonised classification and labelling
CLH 1
Status
Opinion Adopted
Date of intention
01-aug-2012
Withdrawal date
Submitter
Germany
Proposed harmonised classification by the dossier submitter
no classification
Remarks
Date of opinion
06-jun-2014
RAC Opinion
Latest update
02-apr-2019
More information View
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
N-alkoxy-2,2,6,6-tetramethylpiperidine derivatives
Remarks
Date of intention
24-jan-2019
Date of assessment
30-sep-2019
Latest update
04-apr-2022
More information View

List entry date: 28-feb-2018

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