Examples of using Applications for authorization in English and their translations into German
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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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Ecclesiastic
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Political
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Computer
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Programming
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Official/political
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Political
Applications for authorizations the centralized procedure.
The preparation and possible updating of the standard document for applications for authorization referred to in Article 4.
Applications for authorizations referred to in paragraph 1 shall contain the following information.
The Commission sees this as a positive signal to other producers ofgenetically modified organisms which will submit applications for authorizations in the future.
Applications for authorization for medicinal products for human use under the centralized procedure.
The Commission shall, in consultation with the Agency, theMember States and interested parties, draw up detailed guidance on the form in which applications for authorization are to be presented.
Applications for authorization need to be handed in within the legal deadlinefor each purpose that is not excluded from the authorization. .
Whereas it is therefore desirable that a system for the mutual supply of information should be established and that Member States should make available to each other on request the particulars andscientific documentation submitted in connection with applications for authorization of plant protection products;
Applications for authorizations and the decisions of the competent authorities must be made available to the public in accordance with the procedures under national law.
Applications for authorization to carry out usual forms of handling must provide all particulars necessary for application of the provisions governing the customs warehousing procedures.
Applications for authorization to remove goods temporarily shall provide all particulars necessary for the application of the provisions governing the customs warehousing procedure.
Applications for authorization to carry out usual forms of handling must provide all particulars necessary for application of the provisions governing the customs warehousing procedure, in particular Article 522(2) and 3.
Applications for authorization of regular services shall be submitted to the competent authorities of the Member State in whose territory the place of departure is situated, hereinafter referred to as the"authorizing authority.
Application for authorization to perform activities involved in product conformity assessment.
Application for authorization to place medicinal products on the market.
Application for authorization.
Step 3: Application for Authorization by Industry.
An application for authorization for a veterinary medicinal product must be accompanied by the particulars and documents referred to in Articles 5, 5a and 7 of Directive 81/851/EEC.
At your first user(Chris here), you have an application for authorization to accept our iPad friend.
Member States shall also require that every application for authorization be accompanied by a programme of operations setting out inter alia the types of business envisaged and the organizational structure of the investment firm concerned.
An application for authorization for a medicinal product for human use must be accompanied by the particulars and documents referred to in Articles 4 and 4a of Directive 65/65/EEC, in the Annex to Directive 75/318/EEC and in Article 2 of Directive 75/319/EEC.
He shall also send the Committee copies of any such authorization which may have been granted by the other Member States in respect of the medicinal product concerned,and shall indicate whether any application for authorization is currently under consideration in any Member State.
APPLICATION FOR AUTHORIZATION TO HOLD A SECOND MEETING OF THE STUDY GROUP ON REINFORCING PRE-ACCESSION STRATEGY- CZECH REPUBLIC, TOGETHER WITH A HEARING OF PROFESSIONAL ORGANIZATIONS(OWN-INITIATIVE)(PRAGUE) EXTERNAL RELATIONS SECTION.
APPLICATION FOR AUTHORIZATION TO HOLD TWO ADDITIONAL STUDY GROUP MEETINGS AND APPOINT EXPERTS TO ASSIST THE CO-RAPPORTEURS FOR THE OPINION ON THE 5th R& TD FRAMEWORK PROGRAMME(1998-2002) SPECIFIC PROGRAMMES ENERGY SECTION.
The authorization for the customs procedure in question or a copy of the application for authorization where the second subparagraph of Article 556(1) applies, except in cases of entry for the customs warehousing procedure or where Articles 568(3), 656(3) or 695(3) apply.
Whereas Articles 6(3) and 28(3) respectively of Regulation(EEC)No 2309/93 require that any application for authorization for a medicinal product or any application for a variation be accompanied by the fee payable to the Agency for the examination of the application; .
Where a Member State notes that an application for authorization submitted is already under active examination in another Member State in respect of that veterinary medicinal product, the Member State concerned may decide to suspend the detailed examination of the application in order to await the assessment report prepared by the other Member State in accordance with Article 254.
The application for authorization must be accompanied by a copy of any authorization obtained in another Member State or in a third country to place the relevant 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.
Once substances in annex XIV have been recorded(or already recorded in the consultation procedure), the supplier immediately confirms that an authorization of the substances in the contractual product is aimed for andinforms us which uses in the application for authorization should be covered.
Article 7(2) of Directive 65/65/EEC, as amended by Directive 93/39/EEC, or Article 8(2) of Directive 817851/EEC, as amended by Directive 93/40/EEC,which lays down that Where a Member state notes that an application for authorization submitted after 1 January 1995 is already under active examination in another Member State in respect of that medicinal product, the Member State concerned may decide to suspend the detailed examination of the application in order to await the assessment report prepared by the other Member State.