intermediates
PREAMBLE: REACH - Registration, Evaluation, Authorisation and Restriction of Chemicals [
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... (41) For reasons of workability and because of their special nature, specific
registration requirements should be laid down for
intermediates.
Polymers should be exempted from
registration and
evaluation until those that need to be
registered due to the risks posed to human health or the environment can be selected in a practicable and cost-efficient way on the
basis of sound technical and valid scientific criteria. ...
... (66) The
Agency should also be empowered to require further information from
manufacturers,
importers or
downstream users on
substances suspected of posing a risk to human health or the environment, including by reason of their presence on the internal market
in high volumes, on the basis of evaluations performed. Based on the criteria for prioritising
substances developed by the
Agency in cooperation with the
Member States a Community rolling action plan for substance
evaluation should be established, relying on Member State competent authorities to evaluate
substances included therein. If a risk equivalent to the level of concern arising from the use of
substances subject to
authorisation arises from the use of isolated
intermediates on site, the competent authorities of the
Member States should also be allowed to require further information, when justified. ...
... (c) non-isolated intermediates; ...
... 8. On-site isolated intermediates and transported isolated intermediates shall be exempted from: ...
... 8. On-site isolated intermediates and transported isolated intermediates shall be exempted from: ...
ARTICLE-6: General obligation to register substances on their own or in preparations [
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... 2. For
monomers that are used as on-site isolated
intermediates or transported isolated
intermediates, Articles
17 and
18 shall not apply. ...
... 2. For
monomers that are used as on-site isolated
intermediates or transported isolated
intermediates, Articles
17 and
18 shall not apply. ...
ARTICLE-17: Registration of on-site isolated intermediates [
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... 3. Paragraph 2 shall apply only to on-site isolated intermediates if the manufacturer confirms that the substance is only manufactured and used under strictly controlled conditions in that
it is rigorously contained by technical means during its whole lifecycle. Control and procedural technologies shall be used
to minimise emission and any resulting exposure. ...
ARTICLE-18: Registration of transported isolated intermediates [
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... 4. Paragraphs 2 and 3 shall apply only to transported isolated
intermediates if the manufacturer or
importer confirms himself or states that he has received confirmation from the user that the synthesis of (an)other substance(s) from
that intermediate takes place on other sites under the following strictly controlled conditions: ...
ARTICLE-19: Joint submission of data on isolated intermediates by multiple registrants [
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... Joint submission of data on isolated intermediates by multiple registrants ...
ARTICLE-28: Duty to pre-register for phase-in substances [
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... 1. In order to benefit from the transitional regime provided for in Article
23 each potential registrant of a phase-in substance in quantities of one tonne or more per year, including without limitation
intermediates, shall submit all the following information to the
Agency: ...
ARTICLE-49: Further information on on-site isolated intermediates [
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... Further information on on-site isolated intermediates ...
... For on-site isolated
intermediates that are used in strictly controlled conditions, neither dossier nor substance
evaluation shall apply. However, where the competent authority of the Member State in whose territory the site is located considers
that a risk to human health or the environment, equivalent to the level of concern arising from the use of
substances meeting the criteria in Article
57, arises from the use of an on-site isolated intermediate and that risk is not properly controlled, it may: ...