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+Article 18 2. |
Article 18 2.A registration for a transported isolated intermediate shall include all the following information:
(a)
the identity of the manufacturer or importer as specified in Section 1 of Annex VI;
(b)
the identity of the intermediate as specified in Sections 2.1 to 2.3.4 of Annex VI;
(c)
the classification of the intermediate as specified in Section 4 of Annex VI;
(d)
any available existing information on physicochemical, human health or environmental properties of the intermediate. Where a full study report is available, a study summary shall be submitted;
(e)
a brief general description of the use, as specified in Section 3.5 of Annex VI;
(f)
information on risk management measures applied and recommended to the user in accordance with paragraph 4. Except in cases covered under Article 25(3), Article 27(6) or Article 30(3), the registrant shall be in legitimate possession of or have permission to refer to the full study report summarised under (d) for the purpose of registration. The registration shall be accompanied by the fee required in accordance with Title IX. 1. Übersicht
1.1 Referenzen1.2 Identifizierte Anforderungen1.3 Zugehörige Standards2. Identifizierte Anforderungen
3. Zugehörige Standards
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