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Prohibition of substances and residue controls March 2011. Overview. Legislation Organizational chart Competent Authority Official control Other programmes. Legislation.
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Overview • Legislation • Organizational chart • Competent Authority • Official control • Other programmes
Legislation • Directive No 96/22/EC concerning the prohibition on the use in stock farming of certain substances having a hormonal or thyrostatic action and of ß-agonists has been implemented in Iceland and will enter into force on 1 November 2011 • Regulation (IS) No 653/2001 on maximum residue limits, as amended implements Regulation (EU) No 2377/90/EEC concerning maximum residue limits (MRLs) of veterinary medicinal products in foodstuffs of animal origin.
Legislation cont´d. • Council Directive 96/23/EC on measures to monitor certain substances and residues thereof in live animals and animal products has been implemented in Iceland and will enter into force on 1 November 2011 • Iceland has drafted a NRCP for the groups of substances detailed in Annex I to the Directive. • The annual monitoring plan and the results are submitted every year to the FVO.
Competent Authority • MAST, under the Ministry of Fisheries and Agriculture is the Competent Authority for monitoring certain substances and residues thereof in live animals and animal products
Official control • MAST is responsible for residues monitoring in live animals and animal products. • The NRCP is based on the total national production and the requirements of Council Directive 96/23/EC. • Samples are taken from all relevant substance groups • Official veterinarians take the samples except some milk samples at farms
Laboratories • Two laboratories in Iceland • Some antibiotics • Heavy metals • Laboratories abroad • Other substances • No reference laboratory for residues in Iceland
Other programmes • MASToperates a monitoring programme for contaminants in feed, fertilizers and seed. Dairy plants operate own control programmes for antibacterial substances and non-compliant results and evidence of follow up investigations by the dairy plants must be reported to the district veterinary officer
Follow – up of non - compliants • In case of non compliant results the MAST NCPR coordinator would contact the DVO of the district where from the sample originates and require him to follow up on the non compliant result. • There have been no non - compliant results in recent years.