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Showing 3401–3410 of 14436 articles for “Art. 515-6”
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…
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…
I. - Claims for compensation under the out-of-court procedure provided for in article L. 1221-14 in respect of the losses defined in the same article are addressed to the Office national d'indemnisati…
The application for an import authorisation must include : a) The name and address of the importer ; b) The nature and quantity of the product being imported; c) Where applicable, 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…
By way of derogation from the provisions of 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…
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.
When the import concerns plasma pastes or labile blood products intended for the preparation of health products, the authorisation referred to in Article D. 1221-58 is issued to the following organisa…
Notwithstanding the provisions 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 pro…
When applying for an import authorisation, the importer must certify, notwithstanding the provisions of g of Article D. 1221-61, that the samples of blood or its components, from which the product for…
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