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Showing 3721–3730 of 9197 articles for “Art. 1352-8”
The declarations provided for in Articles L. 5211-3-1 and R. 5211-65 as well as the communication provided for in Article R. 5211-66 are made to the Agence nationale de sécurité du médicament et des p…
The content and methods of presentation of the declaration are laid down, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé, by order o…
The declaration provided for in article L. 5221-3 is made by the manufacturer or his authorised representative, the importer, distributor or exporter of in vitro diagnostic medical devices. The same n…
Manufacturers who place in vitro diagnostic medical devices on the French market and who do not have their registered office on the territory of a Member State of the European Union or a party to the…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé is notified of any changes to the information contained in the declaration.
The neurosurgical care activity mentioned in 12° of article R. 6122-25 includes the care of patients with a pathology affecting the brain, the spinal cord, the peripheral nerves, their envelopes (skul…
For the neurosurgical treatment of cancerous lesions, the holder of the authorisation to practise neurosurgical care must hold the authorisation mentioned in 18° of article R. 6122-25.
The authorisation provided for in article L. 6122-1 may only be issued to a health establishment or a health cooperation grouping if it has the following facilities on the same site, possibly by agree…
Authorisation to carry out neurosurgical care is not required from a health establishment or a health cooperation group when it holds an authorisation to carry out the surgical care activity mentioned…
The holder of the authorisation to practise neurosurgery ensures at all times, where appropriate by agreement with other health establishments or health cooperation groups, that patients have access t…
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