Article R513-10-11
In the event of a serious adverse reaction likely to be due to a tattooing product, the persons responsible for placing a tattooing product on the market, the health professionals who have observed it…
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Showing 6871–6880 of 52210 articles for “Art. 2332-1°”
In the event of a serious adverse reaction likely to be due to a tattooing product, the persons responsible for placing a tattooing product on the market, the health professionals who have observed it…
Persons who have access to the information referred to in article R. 513-10-12 are bound by professional secrecy under the conditions set out inarticle 226-13 of the French Criminal Code.
Any person wishing to obtain the information provided for in the previous article shall submit a request by post to the address mentioned in 6° of article R. 513-10-5 or by fax or electronically to th…
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 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…
The holder of an authorisation referred to in Article L. 5141-12 must report to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail,…
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 veterinarian registers the medicinal products referred to in the first paragraph of article R. 5141-126 using any recording system that allows immediate presentation at the request of the control…
The application for renewal of a parallel import authorisation must be accompanied, where appropriate, by a list of changes that have occurred since the initial authorisation or the last renewal was i…
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