Voorbeelden van het gebruik van Application for authorisation in het Engels en hun vertalingen in het Nederlands
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Programming
Regulatory assistance for the definition of the content of the application for authorisation within the meaning of Article 6 of Council Regulation(EEC) N° 2309/93.
which is not acceptable for the transport undertakings which have submitted the application for authorisation.
Naturally, you will need the application for authorisation, approval from the guilds
To submit an application for authorisation of feed additives, including the preparation of a dossier accompanied by the particulars and documents referred to in the proposed Regulation.
To submit an application for authorisation of genetically modified food
An application for authorisation to use simplifications,
The application for authorisation and supplementary information from the applicant
The application for authorisation is submitted in accordance with Article 10 of Directive 2001/83/EC
The Regulation concerning the application for authorisation of a feed additive shall be adopted in accordance with the procedure referred to in Article 21 2.
New data were submitted by the producing company in support of an application for authorisation without a time limit of the micro-organism preparation set out in this Regulation.
Member States may not require that any application for authorisation be considered in the light of the economic requirements of the market.
They have submitted an application for authorisation in accordance with Article 3 of this Regulation before 30 June 2001.
trials which are necessary and useful for the application for authorisation, without specifying who carries them out.
The Member State shall decide within 90 days on whether to approve an application for authorisation of a low-risk plant protection product.
New data were submitted by the producing company in support of the application for authorisation without a time limit of the micro-organism.
Where the sponsor so requests, the application for authorisation of a clinical trial,
Disposal, storage and use of existing stocks of biocidal products for which an application for authorisation has not been submitted in accordance with the second subparagraph are allowed until eighteen months after the date on which the inclusion becomes effective.
If an application for authorisation is turned down on the basis that the risks to human health
This legal form ensures that Member States base their assessment of an application for authorisation of a clinical trial on an identical text, rather than on diverging national transposition measures.
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.