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Showing 4301–4310 of 36396 articles for “Art. Décret n° 2015-1437 du 5 novembre 2015”
With the exception of army pharmacists, pharmacists practising in health establishments, when they are responsible for supervising a blood depot mentioned in article R. 1221-20, must, for this activit…
The authorisation referred to in article D. 1221-58 indicates in particular the name and address of the supplier establishment, the natural or legal person responsible for the import and, where applic…
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…
…ists, pharmacists responsible, in application of article L. 1221-10, for monitoring labile blood products intended for direct therapeutic use in blood establishments must be registered in sections G o…
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.
…sufficiently complete to enable healthcare professionals to assess the therapeutic value of the product. Quotations, tables and other illustrations borrowed from medical journals or scientific works,…
…he Armed Forces Blood Transfusion Centre, subject to the provisions of articles R. 1222-47, R. 1222-50 and R. 1222-51.
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…
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