Examples of using The application for authorisation in English and their translations into Swedish
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Ecclesiastic
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Official/political
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Computer
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Programming
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Political
The application for authorisation in accordance with paragraph 1 shall be made▌within 30▌ days of any agreement entered into by a supervised entity to use an index provided by that administrator as a reference to a financial instrument or financial contract▌.
Member States may only use the information contained in the dossier accompanying the application for authorisation for the benefit of another applicant on certain conditions,
The application for authorisation, supplementary information from the applicant,
The application for authorisation to grant compensatory aid as referred to in Titles II and III shall be
II of the assessment report, the application for authorisation of that substantial modification shall be validated in accordance with Article 17.
feed on the market; under the agreed procedure, the application for authorisation would be sent to the competent national authority of a Member State.
which provides for public accessibility of key documents such as the application for authorisation, supplementary information from the applicant
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.
Where the subjects are minors, specific consideration shall be given to the assessment of the application for authorisation of a clinical trial on the basis of paediatric expertise or after taking advice on clinical,
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.
The application for authorisation, supplementary information from the applicant and opinions from the Authority, excluding confidential information,
To ensure that the assessment of the application for authorisation of a clinical trial functions smoothly, Member States should consider
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
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
Where the application for authorisation is made in accordance with Article 163(1), the containers shall be monitored by a person established in
where the applicant has to prove that the application for authorisation is justified by a genuine need35.
at the time of the evaluation of the application for authorisation, it will be verified that these trials were conducted respecting the principles of good clinical practice