Examples of using Application for authorisation in English and their translations into Danish
{-}
-
Official
-
Financial
-
Colloquial
-
Medicine
-
Ecclesiastic
-
Official/political
-
Computer
Second application for authorisation.
The competent authorities of the home Member State shall consult the relevant central bank before accepting or rejecting an application for authorisation or suspending or withdrawing an authorisation. .
Application for authorisation shall be made in writing using the model set out in Annex 67.
New data were submitted by the producing company in support of the application for authorisation without a time limit of the micro-organism.
Every application for authorisation shall be decided on without undue delay.
The provisions referred to in paragraphs 1 to 5 may not require that any application for authorisation be considered in the light of the economic requirements of the market.
An application for authorisation to use simplifications, hereinafter referred to as'the application', shall be made in writing.
Amendments Nos 4 and 5 are also unacceptable because they give undue preference to copy products by granting them authorisation to be placed into circulation even before an application for authorisation has been submitted.
Member States may not require the application for authorisation to be examined in terms of the economic needs of the market.
In particular circumstances the customs authorities may allow the declaration for freecirculation in writing or by means of a data-processing technique using the normal procedure to constitute an application for authorisation, provided that.
They have submitted an application for authorisation in accordance with Article 3 of this Regulation before 30 June 2001.
The periods of protection provided for in Articles 14(11) and39(10) shall not apply to reference medicinal products for which an application for authorisation has been submitted before the date referred to in Article 90, second paragraph.
The application for authorisation is submitted in accordance with Article 10 of Directive 2001/83/EC or Article 13 of Directive 2001/82/EC;
The Agency shall draw up a procedure on the developmentof orphan medicinal products, covering regulatory assistance for the definition of the content of the application for authorisation within the meaning of Article 6 of Regulation(EEC) No 2309/93.
The application for authorisation is accompanied by a programme of activity setting out, inter alia, the organisational structure ofhe management company;
The competent authorities of the Contracting Party in whose territory the place of departure is situated shall examine the application for authorisation of the service concerned and, in the case of its approval, shall forward it to the competent authorities of the Contracting Party(ies) of destination as well as the competent authorities of the Contracting Parties in transit.
The application for authorisation may be made by means of a customs declaration for temporary importation by any other act in accordance with Article 2321.
In particular, with respect to clinical trials conducted outside the Community on medicinal products destined to be authorised within the Community,at the time of the evaluation of the application for authorisation, it should be verified that these trials were conducted in accordance with the principles of good clinical practice and the ethical requirements equivalent to the provisions of the said Directive.
The application for authorisation shall be submitted by the transport operator to the competent authorities of the Contracting Party on whose territory the point of departure is situated.
The granting of an authorisation or the rejection of an application for authorisation for material included in the list, in accordance with the relevant Community legislation;
An application for authorisation has been submitted for isopropyl ester of the hydroxylated analogue of methionine which belongs to the group"analogues of aminoacids" referred to in the Annex to Directive 82/471/EEC.
Proof that the conditions laid down in Article 4 are satisfied shall be established by a certificate concerning the nature and duration of the activity issued by the competent authority or body in the home Member State orin the Member State from where the beneficiary comes which the beneficiary must submit in support of his application for authorisation to pursue the activity or activities in question in the host Member State.
The authorisation shall not be granted unless the application for authorisation is accompanied by a programme of activity setting out, inter alia, the organisational structure of the investment company;
An application for authorisation was submitted for the additive"manganomanganic oxide" as a source of manganese, which belongs to the group of trace elements referred to in part II of Annex C of Directive 70/524/EEC.
At the same time that the application for authorisation is submitted to the Commission, a copy of it shall be sent to the Member State in which the region of provenance or the origin of the material to be prohibited is located.
Application for authorisation shall be made by, or on behalf of, the person who will be responsible for the first placing on the market of a biocidal product in a particular Member State and shall be to the competent authority of that Member State.
When an application for authorisation is submitted to the ethics committee, the regulatory authority should merely be notified and would then have 30 days in which to raise objections, should it think fit.
The assessment of this application for authorisation in respect of the use of this additive for turkeys for fattening shows that the conditions provided for in Directive 70/524/EEC for authorisation without time limit are satisfied.
Where an application for authorisation is made by a person who exports the temporary export goods without arranging for the processing operations, the customs authorities shall conduct a prior examination of the conditions set out in Article 147(2) of the Code on the basis of supporting documents.
Where the application for authorisation is made in accordance with the first subparagraph of Article 497(3)(c), the containers shall be monitored by a person represented in the customs territory of the Community being able to communicate at all times their location and particulars of entry and discharge.