Article D513-11-12
In the event of infringement of the applicable legislative and regulatory provisions, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may suspend or wit…
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Showing 2251–2260 of 9599 articles for “Art. AMF Instruction-Position-Recommendation 2019-12”
In the event of infringement of the applicable legislative and regulatory provisions, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may suspend or wit…
Veterinarians alone are authorised to administer, in the cases provided for in Article L. 5143-4, to equidae declared as being intended for slaughter for human consumption, medicinal products for huma…
The application for authorisation to import a proprietary veterinary medicinal product in parallel is accompanied by a dossier comprising :1° For each presentation, a sample of the proprietary medicin…
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…
I. - The veterinary medicinal product for which parallel import authorisation is requested may differ from the veterinary medicinal product which has obtained marketing authorisation in France, provid…
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…
The application for authorisation to import a veterinary medicinal product in parallel is sent to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environneme…
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…
I.-A proprietary veterinary medicinal product may be imported in parallel with a view to being placed on the market in France if it meets the following conditions: 1° It comes from another Member Stat…
An import authorisation is required for each import operation involving veterinary medicinal products which have undergone all stages of manufacture, including packaging. By way of derogation from the…
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