lexiara

1.

Any manufacturer or importer of a substance appearing on the priority lists referred to in Article 8 (1) and who has submitted the information under Articles 3 and 4 must, within a given time limit, supply the rapporteur with the data and test results concerning that substance referred to in Article 9 (1) and (2) and those referred to in Article 10 (2).

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Source: EUR-Lex (Cellar) · retrieved 2026-10-29 · Text as adopted (Official Journal); later amendments are not incorporated in this text.