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Showing 4821–4830 of 21091 articles for “Art. CA Paris 20-5-2009 n° 08-2432”
The provisions of this section shall apply to biomedical research on labile blood products, without prejudice to the provisions of Title II of Book I of Part One of this Code.
…mediate product resulting from the fractionation of plasma, whatever its level of processing, which cannot be used as it is for administration to humans, and which is intended for the preparation of h…
With the exception of army pharmacists, pharmacists responsible, in application of article L. 1221-10, for monitoring labile blood products intended for direct therapeutic use in blood establishments…
…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…
…lood Transfusion Centre are not subject to the procedure set out in article L. 1222-3 when they are carried out as part of the centre's mission as defined in 3° of article R. 1222-53.
…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…
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