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Showing 4591–4600 of 42602 articles for “Art. L. 210-6”
Any manufacturer having its registered office in France and who, in any Member State of the European Union or party to the Agreement on the European Economic Area, places class I medical devices or cu…
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail sends a warning to the company in question, together with the inspection report o…
Where the authorised body encounters difficulties in implementing the conformity assessment procedures, it shall refer the matter to the Director General of the Agence nationale de sécurité du médicam…
In vitro diagnostic medical devices, other than in vitro diagnostic medical devices undergoing performance evaluation, are classified in two categories: 1° In vitro diagnostic medical devices whose re…
The Director General of the Agence Nationale de Sécurité du Médicament et des Produits de Santé may require the communication of all information essential for checking the accuracy of the advertised c…
Service providers and equipment distributors shall respect the right of persons who are ill or who have an incapacity or disability to consult the healthcare professional of their choice. They are pro…
The Director General of the Agence Nationale de Sécurité du Médicament et des Produits de Santé may require the communication of all information essential for checking the accuracy of the advertised c…
The Managing Director, the Budget Controller, the Accounting Officer and the Chairman of the Scientific Council attend meetings of the Board of Directors in an advisory capacity. The Chief Executive O…
Healthcare-associated infections contracted in a healthcare establishment are known as nosocomial infections.
The accommodation service referred to in this section may be provided by the establishment referred to in article R. 6111-55 or may be delegated to a third party under an agreement. The third party de…
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