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Showing 3751–3760 of 35281 articles for “Art. R 315-8”
In the event of non-conciliation or partial conciliation, the complaint, together with the minutes, is forwarded within three months of the date of receipt by the President of the relevant Central or…
If the regional or central council is responsible for failing to comply with the time limit referred to in article R. 4234-36, the author of the complaint may ask the president of the national council…
During the conciliation meeting, the parties and, where applicable, their representatives are heard by the conciliator(s). A report of total or partial conciliation or a report of non-conciliation is…
If the complaint concerns one of the members of the regional council, this council may ask the president of the national council to designate another regional council to organise the conciliation.If t…
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 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…
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