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Showing 5971–5980 of 22749 articles for “Art. Cass. com. 15 March 2011”
At the end of the Community arbitration procedure implemented in accordance with the provisions of Articles R. 5121-51-8 and R. 5121-51-9, the Director General of the Agence nationale de sécurité du m…
At the end of the procedures provided for in this sub-section, the marketing authorisation is issued or varied by the Director General of the Agence nationale de sécurité du médicament et des produits…
For the purposes of placing a custom-made medical device on the market, the manufacturer shall follow the procedure defined in Article R. 5211-51. The Director General of the Agence nationale de sécur…
Presenting medical devices that do not comply with the provisions of articles R. 5211-12 and R. 5211-17 at scientific or technical meetings, exhibitions or demonstrations without displaying a sign cle…
…tenariat in accordance with the procedures specified by the general regulations of the Autorité des marchés financiers.
…t company's decisions concerning the scheme are lawful. The General Regulations of the Autorité des marchés financiers shall specify the terms and conditions for the application of this I, in particul…
Each decision taken by the sole member in place of the meeting is recorded by him in the register provided for in the third paragraph of Article L. 223-31. The register is kept at the registered offic…
…imit may be temporarily exceeded. In this case, the management company will inform the Autorité des marchés financiers, the custodian and the fund's auditor of the reasons why the limit has been excee…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may prohibit the prescription and supply of a proprietary medicinal product and withdraw it from the mar…
When an application for authorisation concerns a generic veterinary medicinal product of a reference veterinary medicinal product which has not been authorised in France but which has been authorised…
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