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Showing 8261–8270 of 17962 articles for “Art. 5 avr. 2011”
The regional pharmacovigilance centres inform the Agence nationale de sécurité du médicament et des produits de santé on the same day of the reports of adverse reactions likely to be due to a blood-de…
Blood establishments and organisations or companies manufacturing or exploiting blood-derived medicinal products which are aware of information likely to cast doubt on the quality of blood or plasma i…
The correspondent mentioned in article R. 5121-181 who receives the report provided for in article R. 5121-196 immediately forwards it to the regional pharmacovigilance centre. If he is otherwise awar…
…nale de sécurité du médicament et des produits de santé under the conditions set out in articles R. 5121-171 to R. 5121-173.
…entre, if it is located within this establishment, and to the correspondent mentioned in article R. 5121-181 in other cases; 2° When the medicinal product has not been dispensed in an establishment me…
For the purposes of this sub-section, army hospitals and the army blood transfusion centre are regarded as public health establishments and blood transfusion establishments respectively.
The anaesthetic strategy and all the information collected during the operation and during continuous postoperative monitoring are transcribed in a document filed in the patient's medical record.The s…
The post-interventional monitoring room is equipped with medical devices allowing for each station installed: 1° The supply of medical fluids and vacuum suction ; 2° Continuous monitoring of cardiac r…
Patients admitted to a post-interventional monitoring room are cared for by one or more paramedical staff, or midwives for the procedures provided for in 1° of article D. 6124-98, assigned exclusively…
The post-interventional monitoring room is located close to one or more sites where anaesthesia is performed and where grouping is encouraged, in particular operating sectors and sectors where endosco…
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