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Showing 4871–4880 of 39292 articles for “Art. 25-8 III”
If adverse reactions observed in a blood donor or in a recipient are likely to be due to a product mentioned in II of article L. 5311-1 falling within the scope of another vigilance, a copy of the adv…
I. - Any healthcare professional who observes or is aware of post-donation information shall report it without delay to the haemovigilance and transfusion safety correspondent of the blood establishme…
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…
…/she draws up a serious incident report form when the incident only concerns his/her establishment. III. - When the incident concerns both a blood establishment and a healthcare establishment, the hae…
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.
I. - Any healthcare professional who observes or is aware of an adverse reaction occurring in a recipient of labile blood products shall report it without delay to the haemovigilance and transfusion s…
Articles R. 624-1, excluding the first paragraph, and R. 624-2 to R. 624-11 are applicable to receivership proceedings. The verification of claims is carried out by the mandataire judiciaire in the pr…
Articles R. 624-1 to R. 624-11 are applicable to judicial liquidation proceedings. The liquidator performs the functions assigned to the mandataire judiciaire by these provisions.
When the compulsory liquidation is ordered during safeguard or receivership proceedings, the liquidator shall complete the list of claims mentioned in Article R. 624-2. He deposits the completed list…
The liquidator, within two months of taking up his duties, shall submit to the official receiver a statement mentioning the valuation of the assets and the preferential and unsecured liabilities. In t…
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