Article R5141-123-9
The application for authorisation to import a veterinary medicinal product in parallel is sent to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environneme…
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Showing 5351–5360 of 12814 articles for “Art. T. confl. 13-10-2014 n° 3963”
The application for authorisation to import a veterinary medicinal product in parallel is sent to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environneme…
Substances with anti-infectious, anti-parasitic (external and internal), anti-inflammatory, analgesic, neuroleptic, anaesthetic, hormonal or anabolic properties are subject, in application of the last…
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…
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail shall notify the interested party of his decision with regard to the proven or po…
I.-A proprietary veterinary medicinal product may be imported in parallel with a view to being placed on the market in France if it meets the following conditions: 1° It comes from another Member Stat…
…are establishments where operations relating to these medicinal products are likely to be carried out. II - The intention to use the medicinal products defined in I of this article in veterinary medic…
…° The quantities imported; 5° The desired duration of import operations; 6° The purpose of the import. II - The application is submitted : 1° By a veterinarian or a pharmacist, at the request of the p…
…and address of the pharmacy or the professional domicile where the veterinary practice is carried out. The data they contain must appear on a medium which guarantees their permanence and integrity. Th…
An import authorisation is required for each import operation involving veterinary medicinal products which have undergone all stages of manufacture, including packaging. By way of derogation from the…
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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