Article L773-8
…al economic development and" are deleted; 3° In article L. 512-106, the reference to Article L. 511-31 is deleted; 4° In Article L. 512-107, the references to Articles L. 511-31, L. 511-32 and L. 512-…
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Showing 4661–4670 of 21427 articles for “Art. Cass. com. 31 March 2004”
…al economic development and" are deleted; 3° In article L. 512-106, the reference to Article L. 511-31 is deleted; 4° In Article L. 512-107, the references to Articles L. 511-31, L. 511-32 and L. 512-…
…al economic development and" are deleted; 3° In article L. 512-106, the reference to Article L. 511-31 is deleted; 4° In Article L. 512-107, the references to Articles L. 511-31, L. 511-32 and L. 512-…
…urban areas to be revitalised defined in II, companies that are created between 1 January 2018 and 31 December 2023 and, when they are located in the communes mentioned in the sixth paragraph of the…
…ternal event and that all the conditions of Article 101 of Commission Delegated Regulation (EU) No 231/2013 of 19 December 2012 are met.The depositary shall be liable to the AIF or to the unit-holders…
Where the purchaser lays down requirements relating to security of supply, he may in particular request, in the consultation documents, that the tenderer's tender include: 1° certification or document…
…consumer is benefiting from a price reduction comparable to that of sales, as defined in Article L. 310-3 of the French Commercial Code, outside their legal period mentioned in the same article L. 310…
I. - Notifications of freedom to provide services sent by investment firms to the Autorité de contrôle prudentiel et de résolution pursuant to Article L. 532-24 shall include the following information…
…rocedures laid down by decree in the Conseil d'Etat issued after consultation with the Autorité des marchés financiers. However, subject to a limit of 10% of the share capital per year, the Extraordin…
…r an in vitro diagnostic medical device or its accessory under the conditions set out in article L. 3135-1. The manufacturer of a medicinal product, a medical device or its accessory or an in vitro di…
The presence of an information leaflet for the user in the packaging of any medicinal product or product is compulsory, unless the information referred to in article R. 5121-149 appears directly on th…
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