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Showing 2871–2880 of 52884 articles for “Art. n° 16-10.271 FS-PBI — RJDA 1/18 n° 79”
The CE mark is affixed under the responsibility of the manufacturer or his authorised representative. Its form and dimensions are laid down by order of the Minister for Health. The CE marking must be…
At the request of the Director General of the Agence nationale de sécurité du médicament et des produits de santé, the manufacturer or its authorised representative shall provide any information relat…
The list of decisions of the Director General referred to in Article L. 5322-2 which are communicated to the Ministers for the Economy, Health and Social Security for information fifteen days before t…
The contract sets out the procedures for evaluating the implementation of the objectives and commitments, and in particular provides for the indicators required for this evaluation.The results of this…
The authorisation holder guarantees that the medical biology tests required for the activity will be carried out within a timeframe compatible with the quality of patient care.
The interventional radiology activity referred to in 21° of article R. 6122-25 includes all medical procedures for diagnostic or therapeutic purposes performed with medical imaging guidance and contro…
Public health establishments that are not on the list of regional hospital centres or local hospital lists are hospital centres.
Minutes of each committee meeting are sent to the Chairman of the Management Board and to the members of the committee within a fortnight. Each year, the chairman of the committee shall give an accoun…
Financial control at the Assistance publique-hôpitaux de Paris is carried out under the conditions laid down by Decree 2012-1246 of 7 November 2012 on public budgetary and accounting management. The s…
The Commission Nationale de Biologie Médicale is chaired by a university professor-hospital practitioner, medical biologist, appointed by order of the Minister for Health, for a renewable term of five…
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