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Regulation (EC) No 396/2005 of the European Parliament and of the CouncilShow full title
Regulation (EC) No 396/2005 of the European Parliament and of the Council of 23 February 2005 on maximum residue levels of pesticides in or on food and feed of plant and animal origin and amending Council Directive 91/414/EEC (Text with EEA relevance)
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- Revised 31/01/202046.61 MB
- Revised 14/12/201948.52 MB
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- Revised 13/08/201957.97 MB
- Revised 01/05/201944.66 MB
- Revised 13/02/201943.90 MB
- Revised 26/01/201936.75 MB
- Revised 05/12/201843.09 MB
- Revised 07/02/201842.76 MB
- Revised 03/11/201724.50 MB
- Revised 20/10/201722.77 MB
- Revised 23/08/201724.31 MB
- Revised 10/05/201724.02 MB
- Revised 19/01/201723.09 MB
- Revised 24/11/201622.39 MB
- Revised 26/08/201622.25 MB
- Revised 10/06/201621.51 MB
- Revised 13/05/201619.79 MB
- Revised 12/02/201620.71 MB
- Revised 28/10/201518.11 MB
- Revised 29/07/201518.21 MB
- Revised 02/07/201512.18 MB
- Revised 18/05/201520.28 MB
- Revised 16/01/201518.71 MB
- Revised 13/11/201415.71 MB
- Revised 02/02/201413.05 MB
- Revised 26/10/201211.99 MB
- Revised 01/01/201211.30 MB
- Revised 01/01/201112.88 MB
- Revised 29/07/201010.89 MB
- Revised 07/06/20107.16 MB
- Revised 07/11/20097.01 MB
- Revised 28/03/20094.58 MB
- Revised 01/09/20084.38 MB
- Revised 10/04/20080.19 MB
- Revised 22/02/20060.19 MB
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Changes over time for: Article 8A
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There are currently no known outstanding effects by UK legislation for Regulation (EC) No 396/2005 of the European Parliament and of the Council, Article 8A.
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[F1Article 8AU.K.The competent authority's opinion on applications concerning MRLs
1.An evaluation report under Article 8 must include the competent authority's reasoned opinion on, in particular, the risks to the consumer and where relevant to animals associated with the setting, modification or deletion of an MRL.
2.The reasoned opinion must include—
(a)an assessment of whether the analytical method for routine monitoring proposed in the application is appropriate for the intended control purposes;
(b)the anticipated LOD for the pesticide/product combination;
(c)an assessment of the risks of the acceptable daily intake or acute reference dose being exceeded as a result of the modification of the MRL;
(d)the contribution to the acceptable daily intake due to the residues in the product for which the MRL was requested;
(e)any other element relevant to the risk assessment.
3.The reasoned opinion must clearly define the basis for each conclusion reached.
4.The competent authority may request supplementary information from the applicant where necessary for the giving of a reasoned opinion.]
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