Source ANSES
Member States, or ECHA at the request of the European Commission,
can propose a restriction at any time. This proposal will then be
evaluated at European level, with the result that an opinion may be
issued either :
fully support the proposed restriction
;
support the proposed restriction, but on condition
that some changes are made;
reject the proposed restriction.
The European Commission will then decide on the legal text of
the new entry, which will appear in Annex XVII of the REACh regulation.
Providing information before or at the restriction proposal stage
can help you better anticipate the changes needed in your company.
Particularly if you need to adapt conditions of use, or set up a substitution
plan.
What's more, this proactive approach allows you to contribute
to the process before the regulatory text is adopted.
Whether you are a manufacturer, an industrial user or a professional
user, you use substances subject to the REACh regulation and likely
to be subject to restrictions
[FIC 0157]
, i.e. listed in Annex XVII of
the regulation.
If you are concerned by a restriction
[FIC 0157]
, but consider
that it is not adapted to the specificities of your company, you can
contribute during the procedure (which lasts 15 to 18 months
[FIC 0157]
) before the adoption of the legal text....