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Showing 8181–8190 of 36882 articles for “Art. Décret 2015-587 du 29-5-2015”
The manufacturer is required to update the risk analysis and management system referred to in Article R. 5211-23-2 by analysing all elements relating to the medical devices he manufactures and taking…
Medical devices must be designed and manufactured, taking into account the generally recognised state of the art, in such a way that, when used in accordance with their intended purpose and under the…
…implantable medical devices manufactured from non-viable tissues of animal origin or non-viable products derived from tissues of animal origin, falling within the scope defined in paragraphs 2 and 4…
…section are specified, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé, by order of the Minister for Health.
The provisions of article R. 5211-21 are applicable to in vitro diagnostic medical devices.
…ossible to guarantee the characteristics and performance referred to in Article R. 5221-15 and to reduce as far as possible the risk to personnel involved in the transport, storage and use of the devi…
…proposal from the Director General of the National Agency for the Safety of Medicines and Health Products, shall specify the conditions for implementing the essential requirements defined in Articles…
…ent of the establishment's medical commission, vice-president ; 2° The chairman of the nursing, re-education and medico-technical care committee; 3° The Director of Social Life and Integration; 4° The…
The centre's accounting officer is the Receiver General of Finances for Paris.
The centre has a social committee. It comprises : 1° The director of the establishment, represented, where applicable, by the director of social life and integration ; 2° The heads of the establishmen…
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