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Showing 4811–4820 of 32219 articles for “Art. Décret 87-713 du 26-8-1987”
…to the haemovigilance and transfusion safety correspondent of the blood establishment where the product was collected. If he is unable to identify the donor, he will report it to any haemovigilance a…
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…
If adverse reactions observed in a blood donor or in a recipient are likely to be due to a product mentioned in II of article L. 5311-1 falling within the scope of another vigilance, a copy of the adv…
…the haemovigilance and transfusion safety correspondent of the health establishment in which the product in question was distributed or issued or in which the product in question was administered. The…
Decisions by the Director General of the Agence nationale de sécurité des médicaments et des produits de santé, following consultation with the Etablissement français du sang and the Armed Forces Bloo…
I. - Any healthcare professional who 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 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.
…ssional who observes or is aware of an adverse reaction occurring in a recipient of labile blood products shall report it without delay to the haemovigilance and transfusion safety correspondent of th…
…ensure the administration of the company and, where applicable, the designated auditors, present or duly summoned.
Articles R. 624-1 to R. 624-11 are applicable to judicial liquidation proceedings. The liquidator performs the functions assigned to the mandataire judiciaire by these provisions.
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