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 5731–5740 of 30455 articles for “Art. Cass. 1ère civ. avis 20-10-2022 n° 22-70.011 B”
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…
…dicate : 1° The name or corporate name, address and position of the natural or legal person responsible for the import ; 2° The country of origin and, if different, the country where the veterinary me…
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…
…veterinary medicinal products which have undergone all stages of manufacture, including packaging. By way of derogation from the provisions of the previous paragraph, veterinary medicinal products at…
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…
…years and include the following information: -the name of the veterinary medicinal product and the batch number; -the date of the prescription; -the identification of the animals; -the diagnosis; -th…
Any modification concerning the elements and documents mentioned in Article R. 5141-130 is submitted for authorisation to the Director General of the Agence nationale de sécurité sanitaire de l'alimen…
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…
…n Article R. 5141-123-12, customs officers check the corresponding parallel import authorisation number on the packaging. If the parallel import authorisation number does not appear on the packaging a…
The certificate accompanying medicated feedingstuffs manufactured in another Member State of the European Union or party to the Agreement on the European Economic Area when they are imported correspon…
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