The Board of Directors may only validly deliberate if at least half of its members with voting rights are present. If the quorum is not reached, the Board is reconvened with the same agenda within fifteen days. It shall then validly deliberate regardless of the number of directors present. Resolutions are passed by a simple majority of the members present. In the event of a tie, the Chairman has the…
The Board of Directors sets the general guidelines for the institution’s policy, in particular those concerning the deployment of the institution’s activities, the promotion of donations and medical and research policy. It also deliberates on the following matters: 1° The general organisation of the institution and its internal regulations; 1° bis The procedures for carrying out transfusion activities and the other activities mentioned in article R. 1222-40 ; 2° The…
The deliberations of the Board of Directors are forwarded to the Minister for Health. Decisions relating to the budget and financial statements are enforceable under the conditions set out in Title III of Decree no. 2012-1246 of 7 November 2012 relating to public budgetary and accounting management. Other decisions are enforceable fifteen days after their receipt by the Minister, unless the Minister has objected. In an emergency, the Minister for…
The Chairman of the Etablissement Français du Sang is appointed by decree for a term of five years. His term of office may be renewed for a further three years. He manages the establishment within the framework of the guidelines defined by the Board of Directors, in accordance with the provisions of article L. 1222-5. It performs all acts that are not reserved to the Board of Directors by virtue…
The Chairman informs the institution’s Board of Directors at its next meeting of : 1° Decisions taken in application of article L. 1222-3 ; 2° Appointments made in application of article L. 1222-6 ; 3° Decisions notified to it by the Director General of the Agence nationale de sécurité du médicament et des produits de santé in application of article L. 1223-13.
The person responsible for compliance, within the Etablissement Français du Sang, with the regulations relating to the quality and safety of blood products referred to in Article L. 1222-2 is responsible for : – ensuring that each unit of blood or blood components, whatever its intended use, is collected, tested and, when intended for transfusion, prepared, stored, distributed or issued in accordance with the legislative and regulatory provisions in force;…
The person in charge must satisfy the conditions for practising medicine or pharmacy and have at least two years’ practical experience in the field of blood transfusion in one or more blood transfusion establishments.
The President of the Etablissement Français du Sang appoints one or more interim persons in charge at the same time as the person in charge. For the period of the replacement, the interim person in charge is granted the same powers and responsibilities as those granted to the person in charge and must exercise them effectively for the duration of the replacement. The temporary responsible person must meet the conditions…
The President of the Etablissement Français du Sang shall send the Director General of the Agence Nationale de Sécurité du Médicament et des Produits de Santé a copy of any instrument appointing the person in charge and the interim persons in charge. When the person in charge is temporarily replaced, the President of the Etablissement Français du Sang shall immediately inform the Director General of the Agency of the name…
For the application of this sub-section to the Armed Forces Blood Transfusion Centre, the responsibilities and tasks assigned to the person in charge are carried out by the Director of the Centre.
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is a Registered Trademark of
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182, rue de Rivoli
75001, Paris France
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Paris Bar Registration n° (Toque) C2396
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