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Showing 61–70 of 35948 articles for “Art. s. R 210-9 · R 123-75 · R 123-124”
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…
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…
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 parallel import authorisation is issued for a period of five years. It specifies the differences mentioned in article R. 5141-123-8 with the speciality that has obtained marketing authorisation in…
By way of derogation from article R. 5141-123, the importation of veterinary medicinal products intended exclusively for animals whose flesh or products are not intended for human consumption is not s…
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…
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…
Practical training in conservation care is provided by thanatopractitioners qualified under the conditions defined in article L. 2223-45 and working in a public authority, company, association or esta…
The provisions relating to the import and export of veterinary medicinal products apply : 1° to medicinal products classified as narcotics or to which the narcotics regulations apply in whole or in pa…
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…
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