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Showing 1611–1620 of 39709 articles for “Art. R 623-5”
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…
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…
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.
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…
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 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…
I.-Any violation observed within the Armed Forces Blood Transfusion Centre of the legislative and regulatory requirements applicable to it, as well as the elements mentioned in article L. 1222-11, may…
The State assumes responsibility, even without fault, for the risks incurred by donors as a result of collection operations carried out by the Armed Forces Blood Transfusion Centre.
The Armed Forces Blood Transfusion Centre is made up of a central structure and external structures, known as blood transfusion sites, located in certain armed forces hospitals.The organisation and op…
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