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Showing 271–280 of 365 articles for “Art. 1221”
For the purposes of this section, :1° Distribution of labile blood products:a) The supply of labile blood products by a blood establishment to other blood establishments, health establishments and hea…
Any importation of a labile blood product or a plasma paste is subject to prior authorisation issued by the Director General of the Agence nationale de sécurité du médicament et des produits de santé.…
In order to assess the extent of the damage and determine whether it can be attributed to the accident, the Director of the Office will, if necessary, arrange for an expert opinion. The doctor respons…
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…
Blood establishments, health establishments and health cooperation groups authorised to store labile blood products intended for therapeutic use must have a procedure for withdrawing any unit of such…
Blood banks are subject to at least one inspection by the regional health agency during the period of validity of the authorisation.
For the application of this section, the Minister of Defence shall exercise the powers conferred on the competent regional health agency for army hospitals, whose technical opinion he may seek if nece…
The Office will decide on the compensation claim within six months of the date on which it receives a complete file, by registered letter with acknowledgement of receipt. The decisions of the Office r…
The aim of transfusion safety is to identify hazards that have caused, are causing or are likely to cause incidents or adverse reactions that have threatened, are threatening or may threaten the healt…
The Agence nationale de sécurité du médicament et des produits de santé provides the Etablissement français du sang and the centre de transfusion sanguine des armées with information relating to the s…
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