Eksempler på brug af Authorized in accordance på Engelsk og deres oversættelser til Dansk
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Investment firms authorized in accordance with this Directive;
The exercise of a new fishery in the CCAMLR Convention Area shall be prohibited unless authorized in accordance with paragraph 6.
Ii credit institutions authorized in accordance with Directives 77/780/EEC and 89/646/ EEC;
However, in certain circumstances and under certain conditions they may be authorized in accordance with Article 92(3)(a) of the Treaty.
A transfer authorized in accordance with this Article shall be published as laid down by national law in the Member State in which the risk is situated.
The following may not, however, be authorized in accordance with paragraph 1.
A transfer authorized in accordance with this Article shall be published, under the conditions laid down by national law, in the Member State in which the risk is situated.
Where the person acquiring it has been authorized in accordance with Article 11 himself to effect a transfer to his country of residence.
Member States shall ensure that homeopathic medicinal products manufactured andplaced on the market within the Community are registered or authorized in accordance with Articles 7, 8 and 9.
When disposal or tipping for the purpose of disposal which might lead to indirect discharge is authorized in accordance with Articles 4 or 5, authorization shall specify in particular:- the place where such disposal or tipping is done.
This iswhy the Commission requires producers of synthetic fibres to adapt to market trends andtechnological developments either without aid or with aid authorized in accordance withthe code.
When direct discharge is authorized in accordance with Article 4(2) and(3) or Article 5, or when waste water disposal which inevitably causes indirect discharge is authorized in accordance with Article 5, the authorization shall specify in particular.
Homeopathic veterinary medicinal products other than those referred to in Article 17(1) shall be authorized in accordance with the provisions of Articles 12 to 15 and Chapter 3.
When direct discharge is authorized in accordance with Article 4(2) and(3) or Article 5, or when waste water disposal which inevitably causes indirect discharge is authorized in accordance with Article 5, the authorization shall specify in particular:- the place of discharge.
Use of the Community transit procedure shall be compulsory for goods carried by sea only where they are carried by a regular shipping service authorized in accordance with Article 313a.
Member States shall ensure that in the field of animal nutrition only additives authorized in accordance with this Directive may be put into circulation and that they may be used only if incorporated in feedingstuffs under the conditions set out in the authorization regulation.
Member States shall ensure that homeopathic veterinary medicinal products manufaaured andmarketed within the Community are registered or authorized in accordance with the provisions of Articles 7, 8 and 9.
The declarant shall, upon written request containingall the necessary information, be authorized in accordance with the conditions and in the manner laid down in Articles 261 and 262, to make the declaration for release for free circulation in a simplified form when goods are presented to customs.
Member States shall ensure that homeopathic veterinary medicinal products manufactured andmarketed within the Community are registered or authorized in accordance with the provisions of Articles 17(1) and(2), 18 and 19.
Where urgent action is essential to protect human or animal health or the environment,a Member State may suspend the use on its territory of a veterinary medicinal product which has been authorized in accordance with this Regulation.
The person responsible for placing the medicinal product on the market shall ensure that suspected unexpected adverse reactions to a medicinal product authorized in accordance with the provisions of Regulation(EEC) No 2309/93, which are not classified as serious, arising in the Community or in a third country, are reported to the competent authorities of all Member States and to the Agency.
No veterinary medicinal product intended for administration to animals, the meat or products of which are intended for human consumption,may be marketed in a Member State unless it has been authorized in accordance with Community legislation.
Experiments shall be performed solely by competent authorized persons, or under the direct responsibility of such a person, or if the experimental orother scientific project concerned is authorized in accordance with the provisions of national legislation.
Member States shall ensure that homeopathic medicinal products manufactured andplaced on the market within the Community are registered or authorized in accordance with Articles 14, 15 and 16, except where the products are covered by a registration or authorization which was granted under national law on or before 31 December 1993 and whether or not that registration or authorization has been renewed after that date.
The veterinary medicinal products intended for administration to food-producing animals have the same qualitative andquantitative composition in terms of active substances as the medicinal products authorized in accordance with Articles 5, 7 and 8 in the host Member State;
Member States shall take all necessary steps to ensure that intermediate products are manufactured only by establishments authorized in accordance with Article 4 and that they are the subject of a declaration to the competent authority.
Where a device incorporates, as an integral part, a substance which, if used separately, may be considered to be a medicinal product within the meaning of Article 1 of Directive 65/65/EEC and which is liable to act upon the body with action ancillary to that of the device,that device must be assessed and authorized in accordance with this Directive.