Article R5141-123-17
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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Showing 641–650 of 61220 articles for “Art. L. 123-11-1”
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…
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…
…ite of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail.
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…
The holder of a parallel import authorisation for a proprietary veterinary medicinal product shall immediately inform the marketing authorisation holder in the country of origin of any serious adverse…
Except where human or animal health grounds preclude it, parallel import authorisation is granted if the following conditions are met:1° The veterinary medicinal product is obtained from a company aut…
Silence on the part of the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail shall constitute refusal of authorisation on expiry of a p…
…ral of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail. It shall mention : 1° The name or corporate name and address of the applicant ; 2° As regards the…
…inal product may be submitted by: 1° A veterinary pharmaceutical establishment mentioned in Article L. 5142-1, other than the holder of the marketing authorisation mentioned in Article L. 5141-5 ; 2°…
…t or veterinary surgeon in charge of a veterinary pharmaceutical establishment mentioned in article L. 5142-1 ; 4° By the promoter of a clinical trial or by the person in charge of an experiment. III-…
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