Commission Regulation (EC) No 1323/2007 of 12 November 2007 amending Annex I to Council Regulation (EC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin, as regards firocoxib
Proposed act with possible EEA relevance
Act under scrutiny by EEA EFTA
Draft Joint Committee Decision (JCD) under consideration
Entry into force of Joint Committee Decision (JCD) pending
Incorporated into the EEA Agreement and in force
Incorporated into the EEA Agreement but no longer in force
Legal status
EU legal act incorporated into the EEA Agreement, but no longer in force in the Agreement
Area (EEA Agreement)
II Technical Regulations, Standards, Testing and Certification
II.XIII Medicinal Products
Joint committee decision (JCD)
063/2008
In force in the EEA
No
Legal Documents
Commission Regulation (EC) No 1323/2007 of 12 November 2007 amending Annex I to Council Regulation (EC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin, as regards firocoxib
Verordnung (EG) Nr. 1323/2007 der Kommission vom 12. November 2007 zur Änderung des Anhangs I der Verordnung (EWG) Nr. 2377/90 des Rates zur Schaffung eines Gemeinschaftsverfahrens für die Festsetzung von Höchstmengen für Tierarzneimittelrückstände in Nahrungsmitteln tierischen Ursprungs in Bezug auf Firocoxib
Kommisjonsforordning (EF) nr. 1323/2007 av 12. november 2007 om endring av vedlegg I til rådsforordning (EØF) nr. 2377/90 om en framgangsmåte i Fellesskapet for fastsettelse av maksimumsgrenser for restmengder av veterinærpreparater i næringsmidler av animalsk opprinnelse med hensyn til firokoksib
History
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