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Showing 1531–1540 of 5961 articles for “Art. n° 14-22224 · CA Paris”
The labelling and, where applicable, the package leaflet of the medicinal products referred to in article L. 5121-13 must bear the following information only: 1° Homeopathic medicinal product in clear…
…marketing authorisation in France, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may, subject to the measures he deems necessary to protect human hea…
…marketing authorisation in France, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may, subject to the measures he deems necessary to protect human hea…
…ollowing information: 1° The name of the medicinal product or product, the strength, the pharmaceutical form and, where appropriate, a reference to the recipient ("infants", "children" or "adults") an…
…ollowing information: 1° The name of the medicinal product or product, the strength, the pharmaceutical form and, where appropriate, the name of the recipient ("infants", "children" or "adults") and,…
…ractices established by decision of the Director General of the Agence nationale de sécurité du médicament et des produits de santé.
…of the company manufacturing the medicinal product; 3° The batch number; 4° The route and, if applicable, the method of administration of the medicinal product; 5° The composition in terms of active…
…e protective shielding provides all the explanations relating to the codes used on the vial and indicates, where applicable, the total or unit quantity of radioactivity for a given time and date as we…
…propriate, the method of administration of the medicinal product; 5° The expiry date; 6° Where applicable, the information required for proper storage of the medicinal product.
…ethods available to them. It also includes, in order, the following information: 1° For the identification of the medicinal product or product: a) The name of the medicinal product or product, the str…
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