Eksempler på brug af Set out in annex i to directive på Engelsk og deres oversættelser til Dansk
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Teschen disease is no longer included in List A. It is therefore appropriate to delete that disease from the list set out in Annex I to Directive 92/119/EEC.
African swine fever should be included in the list set out in Annex I to Directive 92/119/EEC and specific provisions for its control should be laid down in accordance with Article 15 of that Directive. .
This authorisation may be granted only for objective, verifiable reasons andmust be based on one of the grounds set out in annex I to Directive 2001/83/EC.
The possibility of discretionary exclusions of certain categories of depositors set out in Annex I to Directive 94/19/ EC has led to a variety of categories of beneficiaries that have to be identified during the payout procedure.
The lists of bodies or of categories of such bodies governed by public law which fulfil the criteria referred to in the second subparagraph are set out in Annex I to Directive 93/37/EEC.
Member States shall review the authorisation for each plant protection product containing deltamethrin to ensure that the conditions relating to deltamethrin set out in Annex I to Directive 91/414/EEC are complied with.
Points I and III in the nomenclature set out in Annex I to Directive 88/361, and the explanatory notes appearing in that annex, indicate that direct investment in the form of participation in an undertaking by means of a shareholding oi the acquisition of securities on the capital maiket constitute capital movements within the meaning of Article 73b of the Tieaty.
Member States shall review the authorisation for each plant protection product containing ethofumesate to ensure that the conditions relating to ethofumesate set out in Annex I to Directive 91/414/EEC are complied with.
The approved bodies shall issue an EEC typeexamination certificate for each type of power generator for which the sound power level of airborne noise,measured under the conditions set out in Annex I to Directive 79/113/EEC, as amended by Annex I to this Directive, does not exceed the permissible sound power level given in the following table.
After inclusion, Member States should be allowed a reasonable period within which to implement the provisions of Directive 91/414/EEC as regards plant protection products containing deltamethrin, and in particular,to review existing authorisations to ensure that the conditions regarding deltamethrin set out in Annex I to Directive 91/414/EEC are satisfied.
The Commission acknowledges that the use of the machinery concerned could prove hazardous, since standard EN 1495:1997 fails to meet the essential health and safety requirements relating to the design and construction of machinery andsafety components set out in Annex I to Directive 98/37/EC, specifically requirements 1.5.15"Risk of slipping, tripping or falling", 1.7.4"Instructions" and 6.3"Risk of persons falling from the carrier.
Member States shall review the authorisation for each plant protection product containing alpha-cypermethrin, benalaxyl, bromoxynil, desmedipham, ioxynil andphenmedipham to ensure that the conditions relating to those active substances set out in Annex I to Directive 91/414/EEC are complied with.
Having regard to that inclusion, Article 4(1) of Directive 2002/37 requires Member States, first, to review authorisations previously granted for each plant protection product containing ethofumesate, in order to ensure that the conditions relating to that active substance, as set out in Annex I to Directive 91/414, are complied with and, second,to amend or, if necessary, to withdraw those authorisations, in accordance with that directive, before 1 September 2003.
Member States shall review the authorisation for each plant protection product containing 2,4-DB, beta-cyfluthrin, cyfluthrin, iprodione, linuron, maleic hydrazide orpendimethalin to ensure that the conditions relating to this active substance set out in Annex I to Directive 91/414/EEC are complied with.
Member States shall review the authorisation for each plant-protection product containing flumioxazine to ensure that the conditions relating to this active substance set out in Annex I to Directive 91/414/EEC are complied with.
Member States shall review the authorisation for each plant protection product containing paraquat to ensure that the conditions relating to those active substances set out in Annex I to Directive 91/414/EEC are complied with.
Member States shall review the authorisation for each plant protection product containing benzoic acid, flazasulfuron orpyraclostrobin to ensure that the conditions relating to these active substances set out in Annex I to Directive 91/414/EEC are complied with.
Member States shall review the authorisation for each plant protection product containing flurtamone, flufenacet, iodosulfuron, dimethenamid-p, picoxystrobin, fosthiazate orsilthiofam to ensure that the conditions relating to these active substances set out in Annex I to Directive 91/414/EEC are complied with.
Member States are authorised, in accordance with Annex III hereto, to permit the marketing in their territory of seed which neither satisfies the requirements in respect of provenance in Directive 66/404/EEC northe requirements relating to specific purity set out in Annex I to Directive 71/161/EEC, on condition that.
After inclusion, Member States should be allowed a reasonable period within which to implement the provisions of Directive 91/414/EEC as regards plant protection products containing chlorpropham, and in particular,to review existing authorisations to ensure that the conditions regarding those active substances set out in Annex I to Directive 91/414/EEC are satisfied.
After inclusion, Member States should be allowed a reasonable period within which to implement the provisions of Directive[91/414] as regards plant protection products containing ethofumesate, and in particular, to review existing authorisations in accordance with the provisions of Directive[91/414]to ensure that the conditions regarding ethofumesate set out in Annex I to Directive[91/414] are satisfied.
On 28 January 2004, Agrichem brought a complaint before the CTB against those decisions, submitting that it did not have to provide an Annex II dossier or show that it had access to such a dossier, given that, in particular, Article 4(1)of Directive 2002/37 merely required it to comply with the conditions set out in Annex I to Directive 91/414, as amended by Directive 2002/37.
By contrast, the proposed regulation provides for a waiver, i.e. competent authorities can decide not to deduct institution's holdings in other institutions, financial institutions or insurance undertakings at individual level where: the entities are part of the same financial conglom erate; or where they are not part of a financial conglomerate butone of the three methods as set out in Annex I to Directive 2002/87/EC is used.
After inclusion, Member States should be allowed a reasonable period within which to implement the provisions of Directive 91/414/EEC as regards plant protection products containing alpha-cypermethrin, benalaxyl, bromoxynil, desmedipham, ioxynil or phenmedipham, and in particular,to review existing authorisations to ensure that the conditions regarding those active substances set out in Annex I to Directive 91/414/EEC are satisfied.
After inclusion, Member States should be allowed a reasonable period within which to implement the provisions of Directive 91/414/EEC as regards plant protection products containing 2,4-DB, beta-cyfluthrin, cyfluthrin, iprodione, linuron, maleic hydrazide or pendimethalin, and in particular,to review existing authorisations to ensure that the conditions regarding those active substances set out in Annex I to Directive 91/414/EEC are satisfied.