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Showing 191–200 of 37773 articles for “Art. L 1221-19”
I.-The distribution and supply of labile blood products required by health establishments and health cooperation groups authorised to manage a blood depot are carried out by a single blood establishme…
In each region, regional haemovigilance and transfusion safety coordinators carry out their vigilance duties under the conditions defined in article R. 1413-61-4.
I. - Any healthcare professional who observes or is aware of post-donation information shall report it without delay to the haemovigilance and transfusion safety correspondent of the blood establishme…
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…
At the request of the Agence nationale de sécurité du médicament et des produits de santé, the blood establishment shall collect and keep all the information necessary for haemovigilance and transfusi…
Each year, the Agence nationale de sécurité du médicament et des produits de santé draws up a summary report on haemovigilance and transfusion safety. This report is sent to the Minister for Health an…
I. - The health care organisation's medical committee or medical conference may refer any matter relating to the implementation of haemovigilance rules in the health care organisation to the regional…
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.
At the request of the Agence nationale de sécurité du médicament et des produits de santé or the Director General of the regional health agency, or on his own initiative, the regional haemovigilance a…
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