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Commission Regulation (EC) No 2592/2001 of 28 December 2001 imposing further information and testing requirements on the manufacturers or importers of certain priority substances in accordance with Council Regulation (EEC) No 793/93 on the evaluation and control of the risk of existing substances

Commission Regulation (EC) No 2592/2001 of 28 December 2001 imposing further information and testing requirements on the manufacturers or importers of certain priority substances in accordance with Council Regulation (EEC) No 793/93 on the evaluation and control of the risk of existing substances

Regulation (EC) No 2592/2001 Β· Regulation Β· 3 articles

Data as of 2026-07-04 Β· Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. Β· Read the official text β†—

Article 1

The manufacturer(s) and importer(s) of the substances listed in the Annex to this Regulation, who have submitted information in accordance with the requirements of Articles 3, 4, 7 and 9 of Regulation (EEC) No 793/93, shall provide the information and perform the tests indicated in the Annex to this Regulation and shall deliver the relevant results to the Member States designated as rapporteur. The tests shall be performed according to the protocols specified by the Member States designated as rapporteur. The results shall be delivered within the time limits laid down in the Annex.

Article 2

This Regulation shall enter into force on the 20th day following its publication in the Official Journal of the European Communities. This Regulation shall be binding in its entirety and directly applicable in all Member States. Done at Brussels, 28 December 2001. For the Commission Margot WallstrΓΆm Member of the Commission (1) OJ L 84, 5.4.1993, p. 1.

Supplementary provisions

ANNEXSupplementary provisions

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Source: EUR-Lex (Publications Office of the EU), Β© European Union, reuse permitted under Commission Decision 2011/833/EU.

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