Article R5141-123-5
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…
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Showing 3791–3800 of 18871 articles for “Art. CA Douai 12-7-2018 n° 18/00485”
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…
…tial risk to human or animal health within sixty days from the date of receipt of the complete application referred to in Article R. 5141-123-9 . The period mentioned in the previous paragraph is redu…
…antitative and qualitative composition in active ingredients and excipients and the same pharmaceutical form as those of a veterinary pharmaceutical product that has obtained a marketing authorisation…
…al Tax Code, as well as to veterinary medicinal products imported by the person responsible for the care of the animal or animals. In this case, the authorisation specifies the number of operations pl…
…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 those relating…
…llows immediate presentation at the request of the control authorities and does not allow any modification of the data after validation of the registration. These records are kept for five years and i…
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…
…company mentioned in article R. 5142-1 plans to close one of its establishments authorised in application of the provisions of article R. 5142-5, it informs the Agence nationale de sécurité sanitaire…
…travail if the speciality no longer satisfies the conditions of the authorisation. Except in urgent cases, these decisions to suspend or withdraw authorisation are taken only after the authorisation h…
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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