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Directive 98/8/EC of the European Parliament and of the Council (repealed)Show full title
Directive 98/8/EC of the European Parliament and of the Council of 16 February 1998 concerning the placing of biocidal products on the market (repealed)
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- Directives originating from the EU
- 1998 No. 8
- Article 27
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- Revised 01/09/20130.44 MB
- Revised 20/08/20131.15 MB
- Revised 14/03/20131.13 MB
- Revised 17/12/20121.08 MB
- Revised 12/09/20121.05 MB
- Revised 27/07/20121.52 MB
- Revised 31/05/20121.51 MB
- Revised 01/03/20121.50 MB
- Revised 11/10/20110.97 MB
- Revised 16/08/20110.93 MB
- Revised 22/07/20110.92 MB
- Revised 01/03/20111.35 MB
- Revised 30/11/20100.96 MB
- Revised 01/09/20100.88 MB
- Revised 02/03/20100.38 MB
- Revised 18/12/20090.36 MB
- Revised 26/10/20090.35 MB
- Revised 25/08/20090.35 MB
- Revised 26/09/20080.29 MB
- Revised 21/03/20080.27 MB
- Revised 07/03/20080.25 MB
- Revised 20/12/20070.26 MB
- Revised 11/10/20070.26 MB
- Revised 24/04/20070.25 MB
- Revised 19/01/20070.25 MB
- Revised 19/06/20060.30 MB
- Revised 20/11/20030.24 MB
- Revised 14/05/19980.24 MB
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Article 27Commission procedures
1.When the Commission receives from a Member State either:
(a)an evaluation and recommendations concerning an active substance in accordance with Article 11(2) and/or an assessment according to Article 10(5), or
(b)a proposal to refuse an authorisation or a registration and an explanatory document in accordance with Article 4(4),
it shall allow a period of 90 days during which other Member States and the applicant may submit comments to it in writing.
2.At the end of the period for comment, the Commission shall, on the basis of:
the documents received from the Member State evaluating the dossiers and,
any advice obtained from advisory scientific committees,
comments received from other Member States and the applicants and,
any other relevant information,
prepare a draft for decision in accordance with the relevant procedures laid down in Article 28(2) or 28(3).
3.The Commission shall ask the applicant and/or his authorised representative to submit remarks to it, unless a favourable decision is envisaged.
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