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Showing 9331–9340 of 24302 articles for “Art. IV”
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…
…red by the same company or by an associated company or working under licence with the same quantitative and qualitative composition in active ingredients and excipients and the same pharmaceutical for…
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…
…origin ; b) The name of the medicated feed, the rate of incorporation of the premix and the qualitative and quantitative composition of the feed fraction.
…horisation for a series of import operations envisaged over a maximum period of one year and for a given overall quantity. The same applies to veterinary medicinal products intended for storage in a n…
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…
…llow any modification of the data after validation of the registration. These records are kept for five years and include the following information: -the name of the veterinary medicinal product and t…
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…
…sation or the last renewal was issued. Where the initial authorisation was granted for a period of five years in accordance with article R. 5141-123-12 of the Public Health Code, the application for r…
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