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Showing 891–900 of 19225 articles for “Art. Cass. com. 20 Oct. 2007”
The labelling of a medical device given to the end user or patient, the accompanying leaflet and any other information relating to its operation or use must include a version written in French.
The manufacturer may instruct his authorised representative to initiate the procedures mentioned in 1°, 2°, 4° and 5° of article R. 5221-19.
When informed of one of the events mentioned in Article L. 5212-2, the Director of the Agence nationale de sécurité du médicament et des produits de santé (French National Agency for the Safety of Med…
The information provided for in I and II of Article L. 5232-5 shall be made available in a dematerialised format, accessible free of charge and reusable in such a way as to allow aggregation. To this…
…ronic signature has been affixed in accordance with the provisions of the aforementioned Decree No. 2017-1416 of 28 September 2017.
The establishment organises the referral of patients who do not require treatment by the emergency department to another care structure or to a social or medico-social structure, in accordance with pr…
The National Committee makes its decisions on the basis of applications. Project promoters are heard by the rapporteur at their request. They may also be heard by the relevant section of the National…
The bariatric surgery care activity referred to in 3° of the I of article R. 6123-202 consists of the surgical management of patients suffering from obesity by means of surgical procedures set by orde…
…activity are performed by a surgeon in the interventional sector mentioned in 1° of article R. 6123-204.
In order to be authorised for "care without consent" and to take charge of adults in care without consent, the holder must be authorised for "adult psychiatry". In order to be authorised for "care wit…
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