Article R2213-43
Where, in exceptional circumstances, certain provisions of this sub-section encounter difficulties in application, the Minister for the Interior and the Minister for Health shall provide for them by m…
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Showing 3051–3060 of 8300 articles for “Art. n° 10-24.180”
Where, in exceptional circumstances, certain provisions of this sub-section encounter difficulties in application, the Minister for the Interior and the Minister for Health shall provide for them by m…
The provisions of article R. 4113-110 are applicable, when they are not members of the health professions, to members of the boards and committees sitting with the Agency and to persons occasionally c…
The parallel import authorisation is granted for a period of five years. It specifies the differences mentioned in articles R. 5121-117 to R. 5121-119 with the speciality that has obtained marketing a…
Private individuals may only import a medicinal product in a quantity compatible with personal therapeutic use for a period of treatment not exceeding three months under normal conditions of use, or f…
The application for renewal of the parallel import authorisation must be submitted no later than three months before the expiry date of the parallel import authorisation. It must be accompanied by a d…
The certificates referred to in Article L. 5124-11 are issued by the Director General of the Agence nationale de sécurité du médicament et des produits de santé. These certificates are valid for three…
Except where there are public health reasons for not doing so, parallel import authorisation is granted if the following conditions are met: 1° The proprietary medicinal product is obtained from an au…
For pharmaceutical products with a parallel import authorisation, Customs officers check the import authorisation number on the packaging. If this number does not appear on the packaging at the time o…
The declaration provided for in the fourth paragraph of Article L. 5124-11 shall be sent to the Agence nationale de sécurité du médicament et des produits de santé by any means capable of providing a…
The application must be accompanied by : 1° For medicinal products imported for research involving the human person, an acknowledgement of receipt of the application sent to the Agence nationale de sé…
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