Article R1221-54
…ception of army pharmacists, pharmacists responsible, in application of article L. 1221-10, for monitoring labile blood products intended for direct therapeutic use in blood establishments must be reg…
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Showing 2761–2770 of 51907 articles for “Art. R. 521-5 to R. 521-11”
…ception of army pharmacists, pharmacists responsible, in application of article L. 1221-10, for monitoring labile blood products intended for direct therapeutic use in blood establishments must be reg…
The information contained in the promotional communication is accurate, up-to-date, verifiable and sufficiently complete to enable healthcare professionals to assess the therapeutic value of the produ…
…Sang submits the draft regional plan for an opinion, by any means which confers a date of receipt, to each regional health agency concerned and to the Minister for Health, as well as, where an army h…
The State assumes responsibility, even without fault, for the risks incurred by donors as a result of collection operations carried out by the Armed Forces Blood Transfusion Centre.
The Armed Forces Blood Transfusion Centre is made up of a central structure and external structures, known as blood transfusion sites, located in certain armed forces hospitals.The organisation and op…
…e under the conditions set out in article L. 1231-3 sits on one of the sites designated by the latter. The list of sites is communicated to the donor by the health establishment in which the removal i…
A copy of the complete dossier is sent by the Director General of the Agence nationale de sécurité du médicament et des produits de santé to the Director General of the Agence de la biomédecine. The D…
Within two months of the date on which the dossier is deemed to be complete, the Minister for Research and, where applicable, the Director General of the Regional Health Agency may, in the cases provi…
Any change in the information contained in the declaration file that is likely to result in a substantial change in the conditions under which the declared activities are carried out, in particular a…
The dossier is deemed to be complete if, within one month of receipt, the Minister responsible for research or, where applicable, the Director General of the regional health agency, has not informed t…
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