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+Article 22 1. |
Article 22 1.Following registration, a registrant shall be responsible on his own initiative for updating his registration without undue delay with relevant new information and submitting it to the Agency in the following cases:
(a)
any change in his status, such as being a manufacturer, an importer or a producer of articles, or in his identity, such as his name or address;
(b)
any change in the composition of the substance as given in Section 2 of Annex VI;
(c)
changes in the annual or total quantities manufactured or imported by him or in the quantities of substances present in articles produced or imported by him if these result in a change of tonnage band, including cessation of manufacture or import;
(d)
new identified uses and new uses advised against as in Section 3.7 of Annex VI for which the substance is manufactured or imported;
(e)
new knowledge of the risks of the substance to human health and/or the environment of which he may reasonably be expected to have become aware which leads to changes in the safety data sheet or the chemical safety report;
(f)
any change in the classification and labelling of the substance;
(g)
any update or amendment of the chemical safety report or Section 5 of Annex VI;
(h)
the registrant identifies the need to perform a test listed in Annex IX or Annex X, in which cases a testing proposal shall be developed;
(i)
any change in the access granted to information in the registration. The Agency shall communicate this information to the competent authority of the relevant Member State. 1. Resumen
1.1 Referencias1.2 Requisitos identificados1.3 Estándares relacionados2. Requisitos identificados
3. Estándares relacionados
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