Article R5141-123-10
…on, a sample of the proprietary medicinal product which has obtained marketing authorisation in France and a sample of the proprietary medicinal product marketed in the country of origin, which is int…
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Showing 2921–2930 of 12941 articles for “Art. CE 9-12-1998 n° 183418”
…on, a sample of the proprietary medicinal product which has obtained marketing authorisation in France and a sample of the proprietary medicinal product marketed in the country of origin, which is int…
…accompanied by the animal or animals for which the medicinal products are intended;3° The import concerns only veterinary medicinal products other than immunological medicinal products;4° The quantity…
…may differ from the veterinary medicinal product which has obtained marketing authorisation in France, provided that these differences have no therapeutic impact and do not entail any risk to public…
Except where human or animal health grounds preclude it, parallel import authorisation is granted if the following conditions are met:1° The veterinary medicinal product is obtained from a company aut…
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…
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…
I.-The request for an import authorisation sent to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail must indicate : 1° The name or…
…s carried out and the quantity imported during the period. The authorisation is returned to the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail as soon as th…
…package leaflet referred to in Articles R. 5141-76 to R. 5141-78 and, with regard to pharmacovigilance, in Articles R. 5141-77 to R. 5141-78. 5141-73 to R. 5141-75, and the package leaflet mentioned i…
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…
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