Article R5141-123-9
…roduct which has obtained marketing authorisation in France, its name within the meaning of Article R. 5141-1, and the number of this authorisation; 3° With regard to the veterinary medicinal product…
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Showing 611–620 of 31323 articles for “Art. s. R. 123-53”
…roduct which has obtained marketing authorisation in France, its name within the meaning of Article R. 5141-1, and the number of this authorisation; 3° With regard to the veterinary medicinal product…
…eleased in accordance with Article 55 of the same Directive;3° Subject to the provisions of Article R. 5141-123-8, the content by weight, by volume or by number of dosage units, the summary of product…
…presupposes that it is signed by the authorising officer or his delegate, in the same way as an order. However, the authorising officer is not obliged to sign a resolution submitted to the accountant…
…tle are complied with, in particular those relating to possession and supply referred to in Article R. 5141-112, labelling referred to in Articles R. 5141-73 to R. 5141-75, and the package leaflet ref…
…ain subject to the specific provisions relating to them respectively, which are set out in articles R. 5132-78, R. 5132-27 and R. 5132-91.
…tion holder in the country of origin of any serious adverse reaction, within the meaning of Article R. 5141-92, concerning the imported proprietary medicinal product, as soon as he is aware of it.
…and protocol for the experiment, a copy of the authorisation to experiment provided for in article R. 214-93 of the Rural and Maritime Fishing Code obtained by the person responsible for the experime…
The administrative authority referred to in articles L. 1237-19-3 to L. 1237-19-5, L. 1237-19-7 and L. 1237-19-8 is the regional director of companies, competition, consumption, labour and employment…
The application for authorisation to import a proprietary veterinary medicinal product in parallel is accompanied by a dossier comprising :1° For each presentation, a sample of the proprietary medicin…
I. - The veterinary medicinal product for which parallel import authorisation is requested may differ from the veterinary medicinal product which has obtained marketing authorisation in France, provid…
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