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Showing 4951–4960 of 40666 articles for “Art. s. L 237-16 · L 237-17 · L 237-26”
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…
In order to comply with the requirements relating to design and manufacture, in vitro diagnostic medical devices are designed, manufactured and packaged in such a way as to meet the following objectiv…
The reports, whether mandatory or optional, provided for in articles R. 5212-14 and R. 5212-15 are made by manufacturers or their representatives, users or third parties who observe or are aware of in…
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 interventions of the SMUR and those of the SMUR branches mentioned in article R. 6123-5 are triggered and coordinated by the SAMU. The mobile emergency and resuscitation structure team informs the…
The emergency medical aid structure has in particular : 1° A room equipped with telecommunications allowing it to be in permanent contact with the SAMU and its own intervention teams; 2° When it has t…
The hierarchical authority shall offer all members of staff, on their appointment and as often as necessary thereafter, an interview devoted to the prevention of situations of conflict of interest. If…
Committee members must be of French nationality and enjoy their civil and political rights.
In authorised establishments and in liaison with their directors, the medical managers of transplant activities and those of intensive care and continuous monitoring units draw up agreements defining…
The healthcare establishment has a paediatric continuous monitoring unit; this may specialise in organ transplants in accordance with the provisions of article R. 6123-38-7. The intensive care activit…
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