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Showing 1621–1630 of 11873 articles for “Art. CE 14-10-2015 n° 374440”
The regional directorate for youth, sport and social cohesion provides the committee's secretariat.
The presence of an information leaflet for the user in the packaging of any medicinal product or product is compulsory, unless the information referred to in article R. 5121-149 appears directly on th…
…intended to be supplied directly to the patient or when it is made available to the patient on an exceptional basis, in particular due to the unavailability of a medicinal product with a marketing aut…
…the following 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…
…the following 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")…
The marketing authorisation holder must comply with the good package leaflet practices established by decision of the Director General of the Agence nationale de sécurité du médicament et des produits…
…visions is not immediately available when authorisation is granted, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may, at the justified request of the…
For medicinal products containing radionuclides, in addition to the information provided for in article R. 5121-140, the labelling of the protective shielding provides all the explanations relating to…
The labelling of the medicinal products mentioned in II of article L. 5121-12-1 includes at least the following information: 1° The name of the medicinal product or, where appropriate, its code name o…
The package leaflet is drawn up in accordance with the summary of product characteristics. It includes a standard text, expressly inviting patients to report any suspected adverse reaction to their do…
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