Guidance on registration - ECHA - Europa
Guidance on registration - ECHA - Europa
Guidance on registration - ECHA - Europa
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<str<strong>on</strong>g>Guidance</str<strong>on</strong>g> <strong>on</strong> registrati<strong>on</strong><br />
Versi<strong>on</strong> 2.0 May 2012 119<br />
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Evaluati<strong>on</strong>:<br />
- Ensure a harm<strong>on</strong>ised approach. Set priorities and take decisi<strong>on</strong>s.<br />
- C<strong>on</strong>duct dossier evaluati<strong>on</strong> of registrati<strong>on</strong>s including testing proposals and other<br />
selected registrati<strong>on</strong>s.<br />
- Substance evaluati<strong>on</strong>: Propose draft Community rolling acti<strong>on</strong> plans, coordinate the<br />
substance evaluati<strong>on</strong> process.<br />
- Take decisi<strong>on</strong>s <strong>on</strong> testing proposals.<br />
Substances in articles: take decisi<strong>on</strong>s <strong>on</strong> notificati<strong>on</strong>s.<br />
Authorisati<strong>on</strong>/restricti<strong>on</strong>s: manage the process and provide opini<strong>on</strong>s. Suggest priorities.<br />
Secretariat for the Forum and Committees.<br />
Take decisi<strong>on</strong>s <strong>on</strong> access to submitted data.<br />
Publish certain specified data <strong>on</strong> a publicly accessible database.<br />
Deal with complaints and appeals.<br />
IV. Commissi<strong>on</strong>:<br />
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Take decisi<strong>on</strong>s <strong>on</strong> further informati<strong>on</strong> needs under the evaluati<strong>on</strong> process where there<br />
is no unanimous agreement by the Member State Committee.<br />
Include substances into the authorisati<strong>on</strong> system.<br />
Take decisi<strong>on</strong>s <strong>on</strong> granting or rejecting authorisati<strong>on</strong>s.<br />
Take decisi<strong>on</strong>s <strong>on</strong> restricti<strong>on</strong>s.<br />
V. All stakeholders including trade or industry associati<strong>on</strong>s, NGOs, and the public:<br />
The following are possibilities/opti<strong>on</strong>s for stakeholders:<br />
Access to n<strong>on</strong>-c<strong>on</strong>fidential informati<strong>on</strong> via the <strong>ECHA</strong> website.<br />
Request access to informati<strong>on</strong>.<br />
Evaluati<strong>on</strong>: submit scientifically valid, relevant informati<strong>on</strong> and studies addressed by<br />
the testing proposal published <strong>on</strong> the <strong>ECHA</strong> website.<br />
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Authorisati<strong>on</strong>:<br />
- Provide comments <strong>on</strong> substances which <strong>ECHA</strong> has proposed to be prioritised and <strong>on</strong><br />
uses which are to be exempted from the authorisati<strong>on</strong> requirement.<br />
- Provide informati<strong>on</strong> <strong>on</strong> possible alternatives.<br />
Restricti<strong>on</strong>s:<br />
- Provide comments <strong>on</strong> restricti<strong>on</strong> proposals.<br />
- Provide socio-ec<strong>on</strong>omic analysis for suggested restricti<strong>on</strong>s, or informati<strong>on</strong> to<br />
c<strong>on</strong>tribute to <strong>on</strong>e.<br />
- Provide comments <strong>on</strong> draft opini<strong>on</strong>s from <strong>ECHA</strong>’s Committee for Risk Assessment<br />
and Committee for Socio-Ec<strong>on</strong>omic Analysis.<br />
Annankatu 18, P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358 9 686180 | Fax +358 9 68618210 | echa.europa.eu
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