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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.

N,N-dimethylacetamide

EC / List no: 204-826-4 CAS no: 127-19-5
Regulatory Management Option Analysis
RMOA 1
Authority
Commission
Concern
Toxic for reproduction
Status
Concluded
Outcome
Appropriate to initiate regulatory risk management action
Follow-up
Restriction
RMOA conclusion document
Remarks
RMOA covers three aprotic solvents: DMF (EC 200-679-5), DMAC (EC 204-826-4) and NMP (EC 212-828-1)
Date of intention
14/09/2017
Date of RMOA conclusion
25/10/2018
Latest update
26/10/2018
More information View
Regulatory risk management
CLH - Harmonised classification and labelling
CLH 1
Status
Opinion Adopted
Date of intention
31/05/2013
Withdrawal date
Submitter
Netherlands
Proposed harmonised classification by the dossier submitter
Acute Tox. 4, H312
Acute Tox. 4, H332
Repr. 1B, H360D
Remarks
Date of opinion
12/09/2014
RAC Opinion
Latest update
02/04/2019
More information View
SVHC - Substances of very high concern
SVHC 1
Status
Identified SVHC
Date of intention
20/07/2011
Withdrawal date
Submitter
ECHA
Remarks
Scope
Toxic for reproduction (Article 57c)
Date of inclusion in Candidate List
19/12/2011
Latest update
19/12/2011
More information View
Restriction
Restriction 1
Status
Intention
Date of intention
09/12/2019
Withdrawal date
Submitter(s)
Netherlands
Remarks
Stakeholders are requested to provide any information relevant to the Dossier Submitter during the Annex XV Restriction Dossier process, either in any call for evidence or separately during the process. This information will be used, amongst other issues, to determine if any derogations are required for the potential restriction as these cannot be proposed without adequate risk and socio-economic information. If a derogation is not proposed by the Dossier Submitter then it will be incumbent on the relevant stakeholders to do so during any public consultation process with a full risk and socio-economic justification accompanying it.
Details on the scope of restriction
Manufacturers, importers and downstream users of the substance on its own (regardless of whether DMAC, NEP are a (main) constituent, an impurity or a stabilizer) or in mixtures in a concentration equal or greater than 0.3 % shall use in their chemical safety assessment and safety data sheets by [date to be specified] a worker based harmonized Derived No Effect Level (DNEL) value [to be specified] for long-term inhalation exposure and a worker based harmonized DNEL value [to be specified] for long-term dermal exposure. Manufacturers and downstream users are to implement appropriate risk management measures ensuring exposure of workers remains below the specified DNEL(s).
The scope may become wider during the development of the Annex XV in case unacceptable risk is identified for consumers due to DMAC and/or NEP presence in consumer articles (or product formulations below 0.3%).
Restriction report (and annexes)
Opinion of RAC (and minority positions)
Draft opinion of SEAC
Compiled RAC and SEAC opinion (and minority positions)
Adopted restriction/Commission communication
Latest update
15/01/2020
More information View

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