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Showing 3721–3730 of 58403 articles for “Art. 206 and 8”
…ous adverse reaction occurring in a blood donor shall report it without delay to the haemovigilance and transfusion safety correspondent of the blood establishment where the product was collected. If…
The Agence nationale de sécurité du médicament et des produits de santé and the regional haemovigilance and transfusion safety coordinator simultaneously receive serious incident report forms, adverse…
…copy of the adverse reaction report form for this donor or recipient is sent by the haemovigilance and transfusion safety correspondent to the correspondent for the vigilance concerned.
…serves or is aware of post-donation information shall report it without delay to the haemovigilance and transfusion safety correspondent of the blood establishment where the blood donation was made. I…
…édicaments et des produits de santé, following consultation with the Etablissement français du sang and the Armed Forces Blood Transfusion Centre, set the form and content of serious incident report f…
…observes or has knowledge of a serious incident shall report it without delay to the haemovigilance and transfusion safety correspondent of the establishment where the incident took place or to that o…
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.
…curring in a recipient of labile blood products shall report it without delay to the haemovigilance and transfusion safety correspondent of the healthcare establishment in which the product was admini…
Articles R. 624-1, excluding the first paragraph, and R. 624-2 to R. 624-11 are applicable to receivership proceedings. The verification of claims is carried out by the mandataire judiciaire in the pr…
…licable to judicial liquidation proceedings. The liquidator performs the functions assigned to the mandataire judiciaire by these provisions.
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