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.

Cyanoguanidine

EC / List no: 207-312-8 CAS no: 461-58-5
Data generation and assessment
DEv - Dossier evaluation
DEv 1
Scope
Testing Proposal
Status
Under assessment
Decision date
Decision
Latest update
10-Jan-2024
Additional information
More information View
DEv 2
Scope
Targeted
Status
Information requested
Decision date
02-Oct-2023
Decision
Latest update
08-Dec-2023
Additional information
More information View
DEv 3
Scope
Targeted
Status
Information requested
Decision date
23-May-2023
Decision
Latest update
06-Jul-2023
Additional information
More information View
DEv 4
Scope
Targeted
Status
Information requested
Decision date
02-Oct-2023
Decision
Latest update
06-Dec-2023
Additional information
More information View
DEv 5
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 6
Scope
Comprehensive
Status
Follow-up
Decision date
06-Feb-2020
Decision
Latest update
26-Nov-2022
Additional information
This Decision has been partly annulled by the Board of Appeal in its decision in Case No.
A-001-2020. Request for Simulation testing on ultimate degradation in surface water is removed following Board of Appeal decision, whereas requests for Sub-chronic toxicity study (90-day) and Pre-natal developmental toxicity study are upheld by Board of Appeal decision.
More information View
DEv 7
Scope
Comprehensive
Status
Concluded
Decision date
07-Oct-2014
Decision
Latest update
26-Nov-2022
Additional information
More information View
DEv 8
Scope
Testing Proposal
Status
Concluded
Decision date
30-Jul-2013
Decision
Latest update
26-Nov-2022
Additional information
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
Guanidylureas, cyanoguanidines and biguanides
Remarks
Date of intention
03-May-2021
Date of assessment
27-Sep-2021
Latest update
26-Apr-2023
More information View

List entry date: 13-Oct-2018

Export search results to: