Examples of using Submitted in accordance in English and their translations into Hungarian
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Financial
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Programming
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Official/political
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Computer
The EU database shall contain the data and information submitted in accordance with this Regulation.
(a) shall verify that the particulars and documents submitted in accordance with Article 6 comply with the requirements of Directive 2001/83/EC, and shall examine whether the conditions specified in this Regulation for granting a marketing authorisation are satisfied;
The application shall be accompanied by the following particulars and documents, submitted in accordance with Annex I.
(c) a survey of the river basin management plans submitted in accordance with Article 15, including suggestions for the improvement of future plans;
The marketing authorisation shall be refused if,after verification of the particulars and documents submitted in accordance with Article 31, it appears that.
The information on the scheme of authorisation for vine plantings submitted in accordance with Article 33 shall be kept for at least ten wine years following the wine year during which it was submitted. .
Without prejudice to other provisions of Community law, the authorization provided for in Article 3 shall be refused if,after verification of the information and particulars submitted in accordance with Article 28, it appears that.
By way of derogation from paragraphs 1 and 2of this Article, sales notes submitted in accordance with Articles 62 and 63 shall be accepted as an alternative measure to sampling plans.
The group of organisers may, in addition, provide translations into all the official languages of the institutions of the Union of the additional information on the initiative and, if any,a draft legal act referred to in Annex II, submitted in accordance with Article 6(2).
Having regard to the interim report of the UN's Special Rapporteur on freedom of religion and belief,Hans Bielefeldt, submitted in accordance with General Assembly resolution 68/170 on freedom of religion and belief.
(a) shall verify that the particulars and documents submitted in accordance with Article 28 comply with the requirements of Directives 81/851/EEC and 81/852/EEC and examine whether the conditions specified in this Regulation for issuing a marketing authorization are satisfied;
The order for immediateenforcement which the court issues in the cases of a document submitted in accordance with Article 417 CPC is also subject to appeal.
Or, where the results of the additional trials or information do not permit definite conclusions to be drawn, to postpone the decision pending the submission of certain further trials in order toclarify any inconclusive points resulting from the additional trials submitted in accordance with Article 7(4).
Import licences shall be issued for the quantities set out in applications for rice andbroken rice falling within CN code 1006 submitted in accordance with the arrangements laid down in Regulation(EC) No 2352/97, reduced by the following percentage.
The group of organisers may, in addition, provide translations into all the official languages of the institutions of the Union of the additional information on the initiative and, if any,a draft legal act referred to in Annex II, submitted in accordance with Article 6(2).
The marketing authorisation shall be refused if,after verification of the particulars and documents submitted in accordance with Article 6, it appears that the applicant has not properly or sufficiently demonstrated the quality, safety or efficacy of the medicinal product.
(40) Given that there is only one cooperating exporting producer and that the Community industry comprises only one company, specific data relating to these companies have been indexed in order topreserve the confidentiality of the data submitted in accordance with Article 19 of the basic Regulation.
The marketing authorisation shall be refused if,after verification of the particulars and documents submitted in accordance with Article 6, it appears that the applicant has not properly or sufficiently demonstrated the quality, safety or efficacy of the medicinal product.
(n) copies of any marketing authorisation obtained in another Member State or in a third country for the relevant veterinary medicinal product,together with a list of those Member States in which an application for authorisation submitted in accordance with this Directive is under examination.
(a) shall verify that the particulars and documents submitted in accordance with Article 6 comply with the requirements of Directives 65/65/EEC, 75/318/EEC and 75/319/EEC, and examine whether the conditions specified in this Regulation for issuing a marketing authorization for the medicinal product are satisfied;
The PNEC shall be determined from the data on effects on organisms andecotoxicity studies submitted in accordance with requirements of Articles 6 and 20.
Member States shall ensure that a decision on an application submitted, in accordance with the requirements laid down in the Member State concerned, by the holder of a marketing authorization to include a medicinal product in the list of medicinal products covered by the health insurance systems is adopted and communicated to the applicant within 90 days of its receipt.
The Commission shall ensure the publication in the register andon the public website on the European citizens' initiative of the information submitted in accordance with Article 6(2) and the translations submitted in accordance with this paragraph.
To suspend the active substance from the market, with the option of reconsidering the inclusion of the active substance in Annex I after submission of certain additional trials or information in order to clarify any inconclusive pointsresulting from the additional trials or information submitted in accordance with Article 7(4);
Without prejudice to other provisions of Community law, the authorization provided for in Article 3 shall be refused if,after verification of the information and particulars submitted in accordance with Article 6, it appears that the quality, the safety or the efficacy of the medicinal product have not been adequately or sufficiently demonstrated by the applicant.
Copies of any authorization obtained in another Member State or in a third country to place the relevant veterinary medicinal product on the market,together with a list of those Member States in which an application for authorization submitted in accordance with this Directive is under examination.
The total quantity of products for which producers conclude storage contracts may not exceed the quantity stated in theirproduction declaration for the wine year concerned, submitted in accordance with Article 18(1) of Regulation(EC) No 1493/1999, plus any quantities they obtained after the date on which their declaration was submitted and recorded in the registers referred to in Article 70 of Regulation(EC) No 1493/1999.
(iii) modifications to the recommended methods and precautions or emergency measures, as set out in sections 2.3, 2.4 and 2.5 of Annex VIIA, VIIB or VIIC,proposed by the notifier in the technical dossier of the notification submitted in accordance with Article 7(1), 8(1) or 8(2) of Directive 67/548/EEC;
Under the direction of the coordinating Member State referred to in paragraph 2, the Member States concerned shall coordinate their assessment of the application,in particular of the documentation submitted in accordance with Chapter I of Annex XIII, except for Sections 4.2, 4.3 and 4.4 thereof which shall be assessed separately by each Member State concerned.
Any authorisation obtained in another Member State, including a summary of the data contained in periodic safety reports and adverse reactions reports, or in a third country to place the medicinal product on the market,together with a list of those Member States in which an application for authorisation submitted in accordance with this Directive is under examination;