+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

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Título Regulación

1.1 Referencias

1.2 Requisitos identificados

1.3 Estándares relacionados

2. Requisitos identificados

Requisitos
Fuente Requisito

3. Estándares relacionados

Estándares
Fuente Requisito