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Showing 3671–3680 of 17844 articles for “Art. 815-5”
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…
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…
This section applies to plasma pastes and labile blood products intended for the preparation of health products. It also applies to labile blood products for direct therapeutic use included on the lis…
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.
The President of the Etablissement Français du Sang submits the draft regional plan for an opinion, by any means which confers a date of receipt, to each regional health agency concerned and to the Mi…
Exports of labile blood products by the Armed Forces Blood 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…
Regional plans may be amended or repealed by decision of the President of the Etablissement Français du Sang in accordance with the procedure set out in Article R. 1222-50. However, the opinion of the…
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