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 4161–4170 of 27460 articles for “Art. Cass. avis 20-10-2000 n° 20-20013”
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…
I.- Medicinal products covered by the regulations on poisonous substances and containing substances mentioned in 7°, 8° or 9° of article L. 5132-2 are used in veterinary medicine in compliance with go…
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…
I.-When veterinary medicinal products prescribed in accordance with the provisions of article R. 5141-111 are dispensed, the pharmacist or veterinarian must immediately transcribe the dispensing in in…
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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