[ParlTrack]

Proposal for a regulation
Recital 1 a (new)

(1a) In order to protect public health, maximum residue limits should be established in accordance with generally recognised principles of safety assessment, taking into account toxicological risks, environmental contamination, as well as unintended microbiological and pharmacological effects of residues. Other scientific assessments of the safety of substances concerned which may have been undertaken by international organisations or scientific committees established within the Community should also be taken into account.

2008/02/28
Committee: ENVI

Dagmar ROTH-BEHRENDT

Proposal for a regulation
Recital 16

(16) In order to protect human health, maximum residue limits should be established in accordance with generally recognised principles of safety assessment, taking into account toxicological risks, environmental contamination, as well as unintended microbiological and pharmacological effects of residues.deleted

2008/02/28
Committee: ENVI

Dagmar ROTH-BEHRENDT

Proposal for a regulation
Article 9 — paragraph 3

3. Within 15 days of the adoption of the final opinion, the Agency shall forward it to the Commission and, as the case may be, to the Member State ~~or party~~ which made the request, stating the grounds for its conclusions.

2008/02/28
Committee: ENVI

María SORNOSA MARTÍNEZ, Dagmar ROTH-BEHRENDT

Proposal for a regulation
Article 18

Methods for establishing reference points 1. The reference points for action shall be based on the content of an analyte in a sample, which can be detected and confirmed by a reference control laboratories designated in accordance with Regulation (EC) No 882/2004 with an analytical method validated according to Community requirements. In this, the Commission shall be advised by the relevant Community reference laboratory on the performance of analytical methods. 2. The Commission may forward a request to the European Food Safety Authority for a risk assessment as to whether the reference points for action are adequate to protect human health. In those cases the European Food Safety Authority shall ensure that the opinion is given to the CommCirculation of foodstuff for action Member States may not prohibit or impede the import and placing on the market of food of animal origin on grounds related to maximum residue limits where the provission within 210 days after receipt of the request. 3. The risk assessment shall take account of rules to be adopted by the Commission in consultation with the European Food Safety Authority. Those rules, designed to amend non- essential elements of this Regulation by supplementing it, shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 21(3). s of this Regulation and its implementing measures have been complied with. Or. es Article 16 of Commission proposal

2008/02/28
Committee: ENVI

4 Amendments of Dagmar ROTH-BEHRENDT related to 2007/0064(COD)

ParlTrack - 2011-2024