Exemple de utilizare a Referred to in section în Engleză și traducerile lor în Română
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Colloquial
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Medicine
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Ecclesiastic
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Ecclesiastic
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Computer
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Programming
Tenders shall be submitted using the specimen application form referred to in section 2 of Regulation(EC)
For the characteristics referred to in Section 3, data shall be reported in a breakdown by.
(e) explosives, as referred to in section 2.1 of Annex I, placed on the market with a view to obtaining an explosive
The authorization shall specify the investment services referred to in Section A of the Annex which the undertaking is authorized to provide.
(h)'securities' shall mean all instruments referred to in section B of the Annex to Directive 93/22/EEC;
international agreements(i.e. all the instruments referred to in section 1(b));
the quantity in kilograms for each of the products referred to in Section 15.
the total quantity of products referred to in Section 16;
the data of persons referred to in section 4 paragraph.
An application for type approval shall be accompanied by the appropriate specifications and by the certificates referred to in Section VIII of Annex IB.
Such procedures shall not however create a guarantee obligation for the institutions of the other Member States in the cases referred to in Section IIIa.";
(2) After each update authority handing a copy of the document referred to in section.
the articles referred to in section 2.1 of Annex I shall be classified,
the supplier shall apply the bridging principles referred to in section 1.1.3 and in each section of parts 3 and 4 of Annex I for the purposes of the evaluation.
the appropriate tests referred to in Section A paragraph 3 shall be carried out to check their conformity to the relevant basic requirements of this Directive.
which has obtained the certificate of conformity referred to in Section 4 complies with the requirements of the Directive.
stored the tests referred to in Section 9.1 shall be required.
The manufacturer shall take all measures necessary to ensure that the manufacturing process guarantees compliance of the manufactured equipment with the technical documentation referred to in Section 2 and with the requirements of the Directive applicable to such equipment.
Where Sections II and III are applied, Member States shall inform the Commission of the adjusted quotas not later than 15 days after the expiry of the periods referred to in Section V.
the number referred to in section 2 is repeated in section 3.