Article R1161-6
The Director General of the Regional Health Agency must be notified of any change in the coordinator referred to in article R. 1161-3, in the objectives of the programme or in the source of funding fo…
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Showing 4171–4180 of 36099 articles for “Art. s. 1304 to 1304-6 · Art. 1305 · Art. 2367 · Art. 1179”
The Director General of the Regional Health Agency must be notified of any change in the coordinator referred to in article R. 1161-3, in the objectives of the programme or in the source of funding fo…
The provisions of articles R. 1211-2 to R. 1211-5 apply to travel relating to the examinations and care that precede or follow the removal or collection, as well as to travel for the purpose of expres…
…ovided for in article L. 1221-14 in respect of the losses defined in the same article are addressed to the Office national d'indemnisation des accidents médicaux, des affections iatrogènes et des infe…
…ct being imported; c) Where applicable, the name and address of the supplier if he is not the collector, together with his authorisation issued by the local health authorities; d) The name and address…
The authorisation to import labile blood products for direct therapeutic use is issued by the Agence nationale de sécurité du médicament et des produits de santé to the Armed Forces Blood Transfusion…
…f g of Article D. 1221-61, when labile blood products from several samples are imported with a view to a scheduled autologous transfusion and the planned date of the procedure so requires, the importe…
The provisions of Section 4 of Chapter V of Title III of this Book apply to the import and export of blood, its components and derived products for scientific purposes.
…r labile blood products intended for the preparation of health products, the authorisation referred to in Article D. 1221-58 is issued to the following organisations or establishments: 1° The Etabliss…
…ns of the first paragraph of Article D. 1221-58, the import authorisation may be issued by the Director General of the Agence nationale de sécurité du médicament et des produits de santé on the basis…
…an undertaking stating that the imported products comply with the requirements of French regulations. When the application for authorisation concerns a plasma paste, the importer must also provide th…
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