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1.Member States making use of the derogation provided for in Article 1 of this Decision shall ensure that the following conditions are complied with:
(a)continued use is only possible under the conditions that products containing the substance are approved for the intended essential use;
(b)the continued use is only accepted so far as it has no unacceptable effect on human or animal health or on the environment;
(c)all appropriate risk reduction measures are imposed when granting approval;
(d)such biocidal products remaining on the market after 1 September 2006 are relabelled in order to match the restricted use conditions;
(e)where appropriate, Member States shall ensure that alternatives for such uses are being sought by the holders of the approvals or by the Member States concerned, or that a dossier is being prepared for submission in accordance with the procedure laid down in Article 11 of Directive 98/8/EC by 14 May 2008 at the latest.
2.The Member States concerned shall inform the Commission annually on the application of paragraph 1 and in particular on the actions taken pursuant to point (e).
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