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Regulatory management option analysis

The regulatory management option analysis (RMOA) list includes substances for which an RMOA either is under development or has been completed since the start of the implementation of the SVHC Roadmap in February 2013.

For each substance, the table shows the assessing Member State (submitter), the concern, the outcome and the suggested follow-up from the RMOA, 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.

 

Disclaimer to the RMOA list

The responsibility for the content of an RMOA rests with the authority that developed it. It is possible that other authorities do not have the same view, and even develop a further RMOA. Any authority can consequently initiate a regulatory process but should indicate this by appropriate means, such as the Registry of Intentions.

RMOAs and their conclusions are compiled based on available information and may change in light of new information or further assessment.

Nonadecafluorodecanoic acid (PFDA) and its sodium and ammonium salts

EC / List no: - CAS no: -
Concern
Bioaccumulation
Other environmental toxicity
Persistence
Status
Concluded
Outcome
Appropriate to initiate regulatory risk management action
Follow-up
SVHC
Date of intention
18/08/2015
Date of RMOA conclusion
11/12/2015
RMOA conclusion document
Full RMOA document
Remarks
Authority
Sweden
Submitter organisation
Swedish Chemicals Agency
Submitter email
rmo@kemi.se
Submitter phone
Submitter address
Co-submitter(s)
Germany
Latest update
30/01/2019

Help Help
Group members
This group of substance has the following member substances:
Name EC / List no. CAS no. Association
Decanoic acid, nonadecafluoro-, sodium salt - 3830-45-3 Expert judgement
Ammonium nonadecafluorodecanoate 221-470-5 3108-42-7 Expert judgement
Nonadecafluorodecanoic acid 206-400-3 335-76-2 Expert judgement

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