Popis s procjenom regulatornih potreba

Popis s procjenom regulatornih potreba

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.  

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Last updated 21 svibnja 2024. Database contains 5071 unique substances/entries.
The List does not contain any Substances.
Substance name EC / List no CAS no Authority Concern Status Follow-up Date of assessment  
209-544-5
584-84-9
Denmark
Aggregated tonnage
Carcinogenic
Exposure
Mutagenic
Widespread use
Concluded
None
23-ruj-2014
Details
209-544-5
584-84-9
Germany
Bioaccumulation
Carcinogenic
Mutagenic
Persistence
Toxic for reproduction
Concluded
Restriction
23-ruj-2014
Details
209-544-5
584-84-9
ECHA
Under development
CCH
16-sij-2023
Details

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