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 2511–2520 of 61590 articles for “Art. R 581-1 et seq.”
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 vigilance exercised over cosmetic products by the Agence nationale de sécurité du médicament et des produits de santé includes : 1° Receiving and recording serious adverse reaction reports sent by…
A national teleservice called "Le Compte Bénévole" (Volunteer Account), under the responsibility of the ministry in charge of associations, enables the declaration provided for in article R. 5151-16 a…
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…
Title I of Book II of this Part is applicable to Wallis and Futuna, with the exception of Articles R. 1211-1 to R. 1211-11, R. 1211-25 to R. 1211-28-1 and R. 1211-48.
The provisions of this code apply in Mayotte, with the exception of articles R. 311-1 to R. 311-3, D. 312-1, R. 332-4 to R. 332-6.
When the congress of departmental and regional elected representatives of the departments mentioned in article L. 5911-1 meets, the articles R. 3123-1 to R. 3123-8 and R. 4135-1 to R. 4135-8 are appli…
Any company or organisation exploiting a medicinal product or product mentioned in article R. 5132-98 must immediately report any serious case of pharmacodependence, abuse or misuse of this medicinal…
After it has been issued, the parallel import authorisation is suspended or withdrawn by the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du…
The holder of a parallel import authorisation shall immediately inform the holder of the marketing authorisation in the State of origin and the holder of the marketing authorisation for the medicinal…
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