Article 22 / Further duties of registrants
Article 22
Further duties of registrants
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:
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;
any change in the composition of the substance as given in Section 2 of Annex VI;
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;
new identified uses and new uses advised against as in Section 3.7 of Annex VI for which the substance is manufactured or imported;
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;
any change in the classification and labelling of the substance;
any update or amendment of the chemical safety report or Section 5 of Annex VI;
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;
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.