Article R1413-42
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…
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Showing 4041–4050 of 10604 articles for “Art. CA Paris 24-10-2024”
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…
…s published on the Agency's website.The Director General of the Agence nationale de sécurité du médicament et des produits de santé sends a copy of the parallel import authorisation to the holder of t…
…edicinal product in question that may be imported and the period during which the operations may be carried out. Importation may be prohibited by the Director General of the Agence nationale de sécuri…
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…
…19, the contents of the packaging in terms of weight, volume or number of dosage units, the classification in the categories mentioned in Article R. 5121-36, the summary of product characteristics, th…
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 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 date certain by the exporting ph…
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…
…ained marketing authorisation in France, as regards: 1° The period of stability, special storage precautions when these are stricter than those of the proprietary medicinal product which has obtained…
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