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Showing 1171–1180 of 17174 articles for “Art. CE 18-6-2008 n° 285380”
…n which the operations for which authorisation has been granted are carried out operates in compliance with the rules of good practice laid down under the conditions referred to in 3° of Article R. 51…
Medical devices which comply with the standards applicable to them, transposing the harmonised European standards, the references of which have been published in the Journal officiel de la République…
For a new device, the Director General of the Agence nationale de sécurité du médicament et des produits de santé may, at any time and for a period of two years following the declaration provided for…
…ir scientific expertise in the field of health products, on the proposal of the Chief Executive Officer and following a call for candidates made by the Agency; 2° Six leading scientists, including for…
…operation groups managing an in-house pharmacy which provide their own sterilisation of medical devices, whether they subcontract it to another health care organisation with an in-house pharmacy or an…
…person presenting in an emergency situation or referred to it, in particular by the emergency services.
…fied by the activity of the emergency unit, the team also includes a nurse who is responsible for receiving and organising patient care. This nurse implements the referral protocols delegated by the d…
…f of the labour inspection system carry out their duties impartially, without expressing any prejudices in their behaviour, words or actions. They ensure that users in identical situations, whatever t…
A joint order of the Minister for the Merchant Navy and the Minister for Finance and Economic Affairs sets the conditions under which travel allowances will be paid to committee members and, for membe…
…older must ensure, in the context of exposure to ionising radiation, that staff and patients have access to the tools needed to optimise radiation protection. A dedicated echocardiograph must be immed…
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