Article D1221-56
…on the list referred to in 1° of Article L. 1221-8, and to those which are the subject of a biomedical research protocol prior to their inclusion on the aforementioned list. The provisions of this se…
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Showing 6511–6520 of 34876 articles for “Art. CA Douai 4-5-2023 n° 22/00072”
…on the list referred to in 1° of Article L. 1221-8, and to those which are the subject of a biomedical research protocol prior to their inclusion on the aforementioned list. The provisions of this se…
The automated national register instituted by Article L. 1232-1 shall be operated and managed by the Agence de la biomédecine under the conditions laid down in this section.
The information contained in the promotional communication is accurate, up-to-date, verifiable and sufficiently complete to enable healthcare professionals to assess the therapeutic value of the produ…
The provisions of this sub-section do not apply to the Armed Forces Blood Transfusion Centre, subject to the provisions of articles R. 1222-47, R. 1222-50 and R. 1222-51.
…er for Defence. The opinions of the Regional Health Agency, the Minister for Health and, where applicable, the Minister for Defence are forwarded to the President of the Etablissement Français du Sang…
…Health Agency is not required for amendments to the plans relating to fixed collection sites, technical facilities for the preparation of labile blood products and technical facilities for the biologi…
…in article L. 1231-3 sits on one of the sites designated by the latter. The list of sites is communicated to the donor by the health establishment in which the removal is planned. The donor chooses th…
Where the activities referred to in article R. 1243-49 are carried out in separate locations, the organisation may submit several declarations, determining the scope covered by each of them.
…of the complete dossier is sent by the Director General of the Agence nationale de sécurité du médicament et des produits de santé to the Director General of the Agence de la biomédecine. The Directo…
…f the date on which the dossier is deemed to be complete, the Minister for Research and, where applicable, the Director General of the Regional Health Agency may, in the cases provided for in Article…
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