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.

2-methyl-1-(4-methylthiophenyl)-2-morpholinopropan-1-one

ACETOCURE 97; GENOCURE*PMP; IGM 4817; IRGACURE 907; SPEEDCURE 97 EC / List no: 400-600-6 CAS no: 71868-10-5
Data generation and assessment
DEv - Dossier evaluation
DEv 1
Scope
Targeted
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
Targeted
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 3
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 4
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 5
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 6
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 7
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 8
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 9
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 10
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 11
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 12
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 13
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 14
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
DEv 15
Scope
Targeted
Status
Concluded
Decision date
Decision
Latest update
26-Nov-2022
Additional information
ECHA has performed an assessment and did not issue a decision but requested further information informally.
More information View
ED - Endocrine disruptor assessment
ED 1
Authority
Austria
Status
Concluded
Outcome
postponed
Hazard assessment outcome document
Remarks
According to the RMOA conclusion document It is acknowledged that further data generation would be necessary to further clarify the concern for endocrine disruption. However, due to the clear human health concern already identified (Repr 1B) and the high substitution potential for the substance, it is rather recommended to await the impact of the risk reduction measures as proposed in the RMOA.
Concern
Endocrine disruption
Date of intention
02-Apr-2019
Date of hazard assessment
Latest update
05-Nov-2021
More information View
Regulatory risk management
CLH - Harmonised classification and labelling
CLH 1
Status
Opinion Adopted
Date of intention
Withdrawal date
Submitter
MIDU
Proposed harmonised classification by the dossier submitter
Acute Tox. 4, H302
Repr. 1B, H360Df
Aquatic Chronic 2, H411
Remarks
Date of opinion
05-Jun-2015
RAC Opinion
Latest update
02-Apr-2019
More information View
SVHC - Substances of very high concern
SVHC 1
Status
Identified SVHC
Date of intention
17-Jun-2019
Withdrawal date
Submitter
Austria
Remarks
Scope
Toxic for reproduction (Article 57c)
Date of inclusion in Candidate List
16-Jan-2020
Latest update
07-Dec-2021
More information View
Recom - Recommendations for inclusion in the Authorisation List
Recom 1
Intrinsic property
Toxic for reproduction (Article 57c)
Status
Recommended for inclusion in Annex XIV
Recommendation round
11th recommendation
Date of draft recommendation
02-Feb-2022
Date of final recommendation
12-Apr-2023
Final recommendation
Date of inclusion in Authorisation List
Regulation amending Annex XIV
Remarks
More information View
Assessment of regulatory needs
ARN 1
Authority
ECHA
Concern
Status
Under development
Follow-up
CCH
Foreseen regulatory need
Restriction
Summary document
Group name
Photoinitiators (benzoyl radical precursor type)
Remarks
Date of intention
12-Apr-2021
Date of assessment
23-Feb-2022
Latest update
11-Jul-2023
More information View
ARN 2
Authority
Austria
Concern
Toxic for reproduction
Status
Concluded
Follow-up
SVHC
Foreseen regulatory need
Summary document
Group name
Remarks
Date of intention
23-Apr-2018
Date of assessment
08-Jul-2019
Latest update
24-Nov-2021
More information View

List entry date: 28-Feb-2018

Export search results to: