Examples of using Application for authorization in English and their translations into Italian
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Colloquial
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Official
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Medicine
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Financial
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Ecclesiastic
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Ecclesiastic
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Computer
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Programming
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Official/political
The application for authorization shall be submitted,
With effect from 1 January 1998, where a Member State is informed in accordance with point 13 of the third paragraph of Article 5 that another Member State has authorized a veterinary medicinal product which is the subject of an application for authorization in the Member State concerned,
With effect from 1 January 1998, where a Member State is informed in accordance with point 11 of the second paragraph of Article 4 that another Member State has authorized a medicinal product which is the subject of an application for authorization in the Member State concerned,
which the applicant shall submit in support of his application for authorization for the type and duration of the activity or activities in question
of the Code is lodged at the same time as the application for authorization, in accordance with Article 523(1) and 2.
a at the time of the application for authorization, a brief description of the plant to be used for the proposed treatments;
Applications for authorization are the responsibility of the candidate.
Submission of applications for authorization 1.
Applications for authorization for medicinal products for human use under the centralized procedure.
Applications for authorizations for veterinary medicinal products under the centralized 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 procedures.
Member States may require that applications for authorization be submitted in their national
The preparation and possible updating of the standard document for applications for authorization referred to in Article 4.
Applications for authorization shall include a description of the plant containing the necessary information for the purposes of the decision whether to grant authorization in accordance with Articles 3 and 4.
Within this new framework, applications for authorization to place medicinal products on the market will fall within the scope of one of the following Articles.
they may be made available only from the date starting from which applications for authorization may be submitted;
Settlement of disagreements on applications for authorizations for medicinal products for human use under the decentralized procedure.
Settlement of disagreements on applications for authorizations for veterinary medicinal products under the decentralized procedure.
Whereas a fee should be laid down for arbitration services in the event of disagreement between Member States on applications for authorizations submitted under the decentralized procedure;
The Commission sees this as a positive signal to other producers of genetically modified organisms which will submit applications for authorizations in the future.