Procedure completed
Role | Committee | Rapporteur | Shadows |
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Opinion | AGRI | ||
Lead | ENVI | COLLINS Kenneth D. (PSE) |
Legal Basis EC before Amsterdam E 043, RoP 154
Activites
- 1997/03/07 Final act published in Official Journal
- #1990
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1997/03/03
Council Meeting
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1997/03/03
End of procedure in Parliament
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1997/03/03
Act adopted by Council after consultation of Parliament
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1997/02/20
Decision by Parliament, 1st reading/single reading
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T4-0055/1997
summary
In adopting the report by Mr Ken COLLINS (PSE, UK) on the amendment of Regulation 2377/90/EEC establishing maximum residue limits of veterinary medicinal products in foodstuffs of animal origin, Parliament adopted only Amendment 8 to this proposal. This amendment which does not concern the substance of the proposal states that if the potentially most dangerous substances such as pyrazolone derivates, nitromidazoles, arsanilic acid and phenylbutazone are not assessed before 31 December 1997 they will be prohibited within the Community from 1 January 1998. �
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T4-0055/1997
summary
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1997/02/19
Debate in Parliament
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Debate in Parliament
summary
Following the contacts announced the day before, Mr Collins said that a revised motion for a resolution had been accepted by the political groups. This text provided for a vote on Amendment No 8 only which related to Article 14 of the proposal.
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Debate in Parliament
summary
- 1997/02/05 Vote in committee, 1st reading/single reading
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1997/01/15
Committee referral announced in Parliament, 1st reading/single reading
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1996/11/19
Legislative proposal published
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COM(1996)0584
summary
OBJECTIVE : to amend Regulation 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin. SUBSTANCE : the amendments proposed by the Commission aim essentially to: - adapt Regulation (EEC) No 2377/90 by conferring on the European Agency for the evaluation of medicinal products the task of dealing with applications for the establishment, amendment and extension of maximum residue limits and by aligning the decision-making process with respect to the authorization and supervision of medicinal products for veterinary use with that introduced by Regulation (EEC) No 2309/93; - enable the Community to fulfil its obligations under the Agreement on the application of sanitary and phytosanitary measures which emerged from the Uruguay Round, an agreement approved by the Community by Council Decision 94/800/EC; - extend until 1 January 1999 the deadline for reviewing old substances, in order to allow the continuation of their scientific evaluation in the best possible conditions. �
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COM(1996)0584
summary
Documents
- Legislative proposal published: COM(1996)0584
- Committee report tabled for plenary, 1st reading/single reading: A4-0035/1997
- Debate in Parliament: Debate in Parliament
- Decision by Parliament, 1st reading/single reading: T4-0055/1997
- : Regulation 1997/434
- : OJ L 067 07.03.1997, p. 0001
History
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