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Showing 4061–4070 of 53735 articles for “Art. Cass. com. 12 January 1999 · Cass. 1re civ. 20 December 2012 · Cass. com. 29 January 2002 · Cass. com. 3 May 2012”
The recruitment of the people mentioned in article L. 5132-1 on assignment contracts by temporary work integration companies entitles them to financial aid, up to the number of integration posts set b…
…olidarity, with territorial jurisdiction, in accordance with the procedures set out in article R. 5132-1-13. The purpose of this inspection is to ensure that : 1° Carrying out the diagnosis referred t…
…cament et des produits de santé sends the coordination group referred to in Article 27 of Directive 2001/83/EC of the European Parliament and of the Council a list of medicinal products for which he c…
The skills operator authorised in application of article R. 6523-2-10 specifies in an appendix to the statistical and financial statement provided for in article R. 6332-31, for the territory, the amo…
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…
The copy of the import authorisation or temporary use authorisation referred to in article L. 5141-10 is presented during the inspection by the customs officers. For imported veterinary medicinal prod…
…thin sixty days from the date of receipt of the complete application referred to in Article R. 5141-123-9 . The period mentioned in the previous paragraph is reduced to thirty days for applications su…
…omplied 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 referred to…
When the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail notifies the holder of the parallel import authorisation for a proprietary v…
The holder of a parallel import authorisation for a proprietary veterinary medicinal product shall immediately inform the marketing authorisation holder in the country of origin of any serious adverse…
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