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Showing 1961–1970 of 26227 articles for “Art. 2369 to 2372”
…médicament et des produits de santé and the regional haemovigilance and transfusion safety coordinator simultaneously receive serious incident report forms, adverse reaction report forms for donors a…
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…
…re 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 establishment where the bloo…
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…
…care professional who observes or has knowledge of a serious incident shall report it without delay to the haemovigilance and transfusion safety correspondent of the establishment where the incident t…
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.
…an adverse reaction occurring in a recipient of labile blood products shall report it without delay to the haemovigilance and transfusion safety correspondent of the healthcare establishment in which…
If the noise referred to in article R. 1336-5 originates from a public or private worksite, or works involving buildings and their equipment subject to a declaration or authorisation procedure, the di…
The noise measurements referred to in article R. 1336-6 are carried out in accordance with the procedures defined by order of the ministers responsible for health, ecology and housing.
No particular noise may, by its duration, repetition or intensity, be detrimental to the tranquillity of the neighbourhood or to human health, in a public or private place, whether caused by a person…
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