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Showing 1371–1380 of 5023 articles for “Art. 16 juin 2004”
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 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 purpose of the vigilance exercised over the software mentioned in 18° of Article L. 5311-1 and the devices mentioned in 19° of the same article, used in medical biology laboratories, is to monitor…
Any healthcare professional who, in the course of his duties within a health care establishment, observes one or more cases of nosocomial infections, informs, on the one hand, the practitioner respons…
The agenda for meetings of the National Committee is set by the minister(s) responsible for social action, health and social security.
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 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 provisions of Article R. 6123-161 and those of 2° of Article R. 6123-162 do not apply to the heavy equipment mentioned in Article L. 6122-14-1.
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