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Showing 3911–3920 of 42602 articles for “Art. L. 210-6”
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.
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…
The importation of a labile blood product or a plasma paste may be authorised only if the samples of blood or its components from which this product has been prepared meet the requirements of section…
The importer is required to: 1° Ensure that the establishment that collected or took the sample undertakes to pass on any information that could call into question the quality and safety of the produc…
Any person of full age or a minor of at least thirteen years of age may be entered on the register in order to make known their refusal to have organs removed from their body after their death, either…
The list of people who may be appointed by the Agence de la biomédecine to sit on the committee of experts is set by order of the Minister for Health after consultation with the Director General of th…
In order to ensure better use of resources and means in the field of blood transfusion, agreements concerning the collection of blood and its components and the preparation, storage, transfer and exch…
Notwithstanding the provisions of article R. 1221-18, the Armed Forces Blood Transfusion Centre may distribute and supply labile blood products which it alone has available to Armed Forces hospitals f…
The Director General of the Regional Health Agency will notify the applicant of his decision within six months of the date on which the complete application was sent to him. If no decision is taken wi…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé will notify the applicant of his decision within four months of the date on which the application is dee…
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