Article R5141-123-17
The holder of the parallel import authorisation is responsible for placing the product on the market and, in this capacity, ensures that the provisions of this Title are complied with, in particular t…
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Showing 201–210 of 27870 articles for “Art. Cass. 3e civ. 16-10-2013 n° 12-19.352”
The holder of the parallel import authorisation is responsible for placing the product on the market and, in this capacity, ensures that the provisions of this Title are complied with, in particular t…
The veterinarian registers the medicinal products referred to in the first paragraph of article R. 5141-126 using any recording system that allows immediate presentation at the request of the control…
The application for renewal of a parallel import authorisation must be accompanied, where appropriate, by a list of changes that have occurred since the initial authorisation or the last renewal was i…
For veterinary medicinal products with a parallel import authorisation as provided for in Article R. 5141-123-12, customs officers check the corresponding parallel import authorisation number on the p…
After it has been issued, the parallel import authorisation is suspended or withdrawn by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du…
I.- In the event of repackaging, the holder of a parallel import authorisation for a proprietary veterinary medicinal product shall notify the holder of the marketing authorisation for the proprietary…
The provisions relating to the import and export of veterinary medicinal products apply : 1° to medicinal products classified as narcotics or to which the narcotics regulations apply in whole or in pa…
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…
The following have the status of judicial police officers:1° Mayors and their deputies;2° Gendarmerie officers and ranks, gendarmes nominatively designated by order of the ministers of justice and the…
Any medicinal product which does not have a marketing authorisation as referred to in Article L. 5121-8 or an early access authorisation as referred to in Article L. 5121-12 or a compassionate access…
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