Voorbeelden van het gebruik van Authorization referred in het Engels en hun vertalingen in het Nederlands
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Colloquial
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Official
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Ecclesiastic
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Medicine
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Financial
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Computer
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Ecclesiastic
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Official/political
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Programming
The authorization referred to in Article 263 shall be granted provided that.
shall give the authorization referred to in Article 172.
The holder of an authorization referred to in Article 16 shall at least be obliged.
The Directive applies to all Community credit institutions which have obtained the authorization referred to in Council Directive 77/780/EEC summary 1.2.
The holder of an authorization referred to in Article 24 shall at least be obliged to.
Without prejudice to the obligations under Article 2 of the basic Regulation, the holder of the authorization referred to in paragraph 1 above shall comply with following obligations.
The authorization referred to in Article 269(1) shall lay down the specific rules for the operation of the procedure.
Member States shall ensure that the authorization referred to in Article 2 may be acquired only be agree.
The authorization referred to in Article 61(6) shall be granted only to persons who satisfy the following conditions.
The application for an export licence for white sugar shall not be accepted unless the authorization referred to in paragraph 1 is produced
The authorization referred to in Article 272(1) shall lay down the specific rules for the operation of the procedure and shall specify in particular.
any laboratories entrusted by the holder of the authorization referred to in Article 24(1), with the task of carrying out control tests pursuant to Article 10 point 2;
The authorization referred to in Article 269(1) shall be granted to the person concerned provided that the proper conduct of operations is not thereby affected.
state whether they wish their application or tender to stand if the authorization referred to in Article 3(1) is refused.
In order to obtain the authorization referred to in Article 24, the applicant shall meet at least the following requirements.
Member States shall certify that a manufacturer of medicinal products is in possession of the authorization referred to in Article 16 1.
The Commission shall grant the authorization referred to in the preceding paragraph if it finds that the proposed transaction will not give to.
destined for another Member State are accompanied by a copy of the authorization referred to in paragraph 1.
suspend or revoke the authorization referred to in Article 3(1) shall state in detail the reasons on which they are based.
The authorization referred to in paragraph 1 may,
No veterinary medicinal product may be administered to animals unless the authorization referred to above has been issued,
The authorization referred to in paragraph 1 shall be required for both total
The competent surveillance authority, as provided for in Article 56 of the Agreement, shall grant the authorization referred to in paragraph 1 if it finds that the proposed transaction will not give to the persons
The authorization referred to in paragraph 2 shall be limited to those substances which are already covered by the relevant Community legislation on drugs precursors and chemical substances.
on whose behalf it was granted and in which the authorization referred to in Article 3(1)(b) to place the
Manufacturer means the holder of the authorization referred to in Article 16 of Directive 75/319/EEC on behalf of whom the qualified person has performed the specific obligations laid down in Article 22 of that Directive.
Member States shall not impose upon the holder of an authorization referred to in Article 3(1)
Whereas the extent of the authorization referred to in Article 1(1)
Member States shall not impose upon the holder of an authorization referred to in Article 3(1)
Where the authorization referred to in the second subparagraph of Article 238(2)(b)