Examples of using Application for authorization in English and their translations into Dutch
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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
Application for authorization.
Within what period of time must an application for authorization be processed by the FSMA?
Application for authorization to place medicinal products on the market.
It shall be delivered to the undertaking having lodged the application for authorization, along with a certified true copy to the other undertakings.
Our application for authorization to sell medication online at the ARS Languedoc Roussillon has been validated since 2014.
People also translate
That nevertheless does not exclude the agent from approaching the customs authorities provided that the application for authorization is made on behalf of its principal.
Examination of the application for authorization to place proprietary medical products on the market.
the written authorization for the customs procedure in question or a copy of the application for authorization where the second subparagraph of Article 556(1) applies;
An application for authorization for a veterinary medicinal product must be accompanied by the particulars
to change the models of the application for authorization and of the use of the inward processing procedure;
In providing that"the application for authorization shall be lodged by
In addition to the requirements set out in Article 4 of Directive 65/65/EEC, an application for authorization to market a generator shall also contain the following information and particulars.
dispatch have acknowledged receipt of the application for authorization of the shipment. 9.
In addition to the requirements set out in Articles 8 and 10(1), an application for authorization to market a radionuclide generator shall also contain the following information and particulars.
Whereas the introduction of fees must be accompanied by the assurance that a decision will be reached by a given deadline on the application for authorization to put an additive into circulation;
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.
The sole criteria which may be taken Into consideration by the Member States during the examination of an application for authorization are the quality,
From 1 January 1994, Member States shall refuse an application for authorization to place a medicinal product on the market
Under a job-processing contract between two persons established in the Community"the application for authorization shall be lodged by or on behalf of the principal.
An application for authorization for a medicinal product for human use must be accompanied by the particulars
where appropriate, the written authorization of the procedure or a copy of the application for authorization where the second subparagraph of Article 751(1) applies.
The application for authorization must be lodged with the competent authority of the Member State concerned
shall indicate whether any application for authorization is currently under consideration in any Member State.
The application for authorization of a generator must also include the following information
with the exception of the official publication of the application for authorization and the submission of the documents for public inspection see points 9 to 123.
Where the application for authorization relates to goods subject to the commercial policy measures referred to in Article 607(1)(a) it shall not
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.
Furthermore, a Member State should be able to suspend the examination of an application for authorization to place a medicinal product on the market which is currently under active consideration in another Member State with a view to recognizing the decision reached by the latter Member State.
is a Member State, the consignee shall submit an application for authorization to the competent authorities of that Member State using the standard document referred to in Article 20.
Furthermore, a Member State should be able to suspend the examination of an application for authorization to place a veterinary medicinal product on the market which is currently under active consideration in another Member State with a view to recognizing the decision reached by the latter Member State.