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Guidance on registration - ECHA - Europa

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86<br />

<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<br />

7 When and how to update a registrati<strong>on</strong><br />

Aim:<br />

The aim of this chapter is to explain when and how to update a registrati<strong>on</strong>. It<br />

explains all reas<strong>on</strong>s why the registrant should update the registrati<strong>on</strong> <strong>on</strong> his own<br />

initiative and when the authorities can request the registrant to update the<br />

registrati<strong>on</strong> dossier. It also describes what the updating duties for substances<br />

regarded as registered are. If in need of updating his registrati<strong>on</strong> informati<strong>on</strong> the<br />

reader is advised to also c<strong>on</strong>sult Part II of this guidance where detailed practical<br />

instructi<strong>on</strong>s are provided.<br />

Structure: The structure of this chapter is as follows (to be corrected):<br />

WHEN AND HOW TO UPDATE A<br />

REGISTRATION<br />

DUTY TO KEEP<br />

INFORMATION UP-TO-DATE<br />

Secti<strong>on</strong> 7.1<br />

UPDATE ON THE<br />

REGISTRANT'S OWN<br />

INITIATIVE<br />

Secti<strong>on</strong> 7.2<br />

UPDATE AS A<br />

CONSEQUENCE OF<br />

AUTHORITIES’ DECISIONS<br />

Secti<strong>on</strong> 7.3<br />

UPDATE FOR<br />

SUBSTANCES REGARDED AS<br />

BEING REGISTERED<br />

Secti<strong>on</strong> 7.4<br />

7.1 Duty to keep informati<strong>on</strong> up to date<br />

The informati<strong>on</strong> submitted to <strong>ECHA</strong> will have to be kept up to date. It is the resp<strong>on</strong>sibility of<br />

the registrant to update his registrati<strong>on</strong> informati<strong>on</strong> when needed. If the informati<strong>on</strong> to be<br />

updated is part of jointly submitted informati<strong>on</strong>, it will be the lead registrant who will have to<br />

update the registrati<strong>on</strong> <strong>on</strong> behalf of the members of the joint submissi<strong>on</strong>.<br />

In order to update his registrati<strong>on</strong> informati<strong>on</strong>, the registrant will have to update his IUCLID 5<br />

dossier and submit it to <strong>ECHA</strong> through REACH-IT. Where the update relates exclusively to<br />

administrative data such as the identity of the registrant or the compositi<strong>on</strong> of the group of<br />

registrants in a joint submissi<strong>on</strong>, however, the updated informati<strong>on</strong> will be directly reported in<br />

REACH-IT. No update of the IUCLID 5 dossier is required in this case.<br />

There are basically two types of situati<strong>on</strong>s where a registrant needs to update the informati<strong>on</strong><br />

c<strong>on</strong>cerning his registrati<strong>on</strong>:<br />

<br />

update <strong>on</strong> the registrant's own initiative<br />

Registrants are required to report to <strong>ECHA</strong> without undue delay any new relevant<br />

available informati<strong>on</strong> (e.g. new t<strong>on</strong>nage band) c<strong>on</strong>cerning their registrati<strong>on</strong> (Article 22<br />

(1)).<br />

<br />

update as a c<strong>on</strong>sequence of a decisi<strong>on</strong> made by <strong>ECHA</strong> or the Commissi<strong>on</strong><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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