Article R5141-112-3
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…
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Showing 3201–3210 of 34588 articles for “Art. R 561-10”
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…
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…
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…
When the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail notifies the holder of the parallel import authorisation for a proprietary v…
After it has been issued, the parallel import authorisation is suspended or withdrawn by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du…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…
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