Article R4233-38
…r conciliators shall refrain from sitting in the Disciplinary Chamber during the examination of the case for which they have organised conciliation.
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Showing 4551–4560 of 46223 articles for “Art. CA Paris 22 January 2013 · Cass. 1re civ. 3 November 1965 · Cass. 3e civ. 8 January 1992”
…r conciliators shall refrain from sitting in the Disciplinary Chamber during the examination of the case for which they have organised conciliation.
…n 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 of the Minister for Health. This order may provide for spe…
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 disciplinary sanctions applicable to contractual practitioners are: 1° Warning; 2° Reprimand; 3° Temporary exclusion from service for a period not exceeding six months and deprivation of all remun…
…roceedings may be suspended, after receiving the opinion of the chairman of the establishment's medical committee, by decision of the director of the establishment, who shall immediately inform the di…
Each member of the co-ownerships of racehorses or stallions mentioned in Article 8 quinquies depreciates the cost price of its share of ownership in accordance with the procedures laid down in respect…
Under terms specified by the decree provided for in article 706-53-12, the file manager shall directly notify the Ministry of the Interior, which shall immediately forward the information to the compe…
The Office registers the application and, if necessary, requests any missing documents. On receipt of the initial application, the Office informs the manufacturer or manufacturers of the medicinal pro…
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