Article R513-10-12
When the Director General of the Agence nationale de sécurité du médicament et des produits de santé makes a reasoned request, the person responsible for placing the product on the market shall send h…
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Showing 2591–2600 of 28784 articles for “Art. Cass. 3e civ. 12-7-1995 n° 93-20.599”
When the Director General of the Agence nationale de sécurité du médicament et des produits de santé makes a reasoned request, the person responsible for placing the product on the market shall send h…
At the end of the Community arbitration procedure implemented in accordance with the provisions of Articles R. 5141-47-9 to R. 5141-47-11, the Director General of the Agence nationale de sécurité sani…
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…
By way of derogation from article R. 5141-123, the importation of veterinary medicinal products intended exclusively for animals whose flesh or products are not intended for human consumption is not s…
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…
Silence on the part of the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail shall constitute refusal of authorisation on expiry of a p…
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…
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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