Regulatory management option analysis

Regulatory management option analysis

The assessment of regulatory needs list includes substances for which an assessment either is under development or has been completed. 

For each substance, the table shows the assessing authority (submitter), the concern, the status and the suggested follow-up action, and the date of the latest update to the list entry.

Other process details and relevant documents are also available and can be accessed through the ‘Details’ icon for the list entry.

Regulatory Management Option Analysis (RMOA) are assessments of regulatory needs. Publication of RMOA was initiated in February 2013 with the start of the implementation of the SVHC Roadmap. In 2019, authorities and in particular ECHA have moved to address more groups of substances.

The responsibility for the content of an assessment of regulatory needs rests with the authority that developed it. It is possible that other authorities do not have the same view and may develop a further assessment of regulatory needs for the same (group of) substances. Assessment of regulatory needs and their conclusions are compiled based on available information and may change in light of new information or further assessment.  

Ethylenediamine

EC / List no: 203-468-6 CAS no: 107-15-3
Concern
Respiratory sensitiser
Skin sensitiser
Toxic for reproduction
Status
Concluded
Outcome
Appropriate to initiate regulatory risk management action
Follow-up
SVHC
Date of intention
11/12/2012
Date of RMOA conclusion
13/10/2016
RMOA conclusion document
Full RMOA document
Remarks
Authority
ECHA
Submitter organisation
ECHA
Submitter email
rmoa@echa.europa.eu
Submitter phone
+358-9-686180
Submitter address
European Chemicals Agency, Annankatu 18, PO Box 400, FI-00121, Helsinki, Finland
Co-submitter(s)
Latest update
13/10/2016

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