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Showing 4681–4690 of 49555 articles for “Art. L. 125-5 V + jurisprudence”
…my pharmacists, pharmacists practising in health establishments, when they are responsible for supervising a blood depot mentioned in article R. 1221-20, must, for this activity, be registered in sect…
…r, the nature and quantity of the imported product and the intended use. It specifies its period of validity and must be presented during a customs inspection. The import authorisation is valid for a…
…Armed Forces Blood Transfusion Centre, set the form and content of serious incident report forms, adverse reaction report forms for donors and recipients and post-donation information report forms, as…
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.
A plasma paste is any intermediate 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 intend…
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.
…the Minister for Health, as well as, where an army hospital or other element of the army health service is concerned, to the Minister for Defence. The opinions of the Regional Health Agency, the Mini…
…Etablissement Français du Sang in accordance with the procedure set out in Article R. 1222-50. However, the opinion of the Regional Health Agency is not required for amendments to the plans relating…
The State assumes responsibility, even without fault, for the risks incurred by donors as a result of collection operations carried out by the Armed Forces Blood Transfusion Centre.
The director of the centre, chosen from among the army doctors who meet the conditions set out in article R. 1222-9-2, is appointed by the Minister for Defence, after consultation with the Minister fo…
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