Article L811-4
I. - For their application in New Caledonia, Articles L. 717-1, L. 717-4 and Article L. 717-7 of this Code shall read as follows:"Art. L. 717-1. :I. - The use in the course of trade by a third party,…
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Showing 4601–4610 of 36308 articles for “Art. Cass. 3e civ. 16-4-2008 n° 07-15.486”
I. - For their application in New Caledonia, Articles L. 717-1, L. 717-4 and Article L. 717-7 of this Code shall read as follows:"Art. L. 717-1. :I. - The use in the course of trade by a third party,…
The following concession contracts are subject to the rules set out in Title II :1° Services relating to the acquisition or rental, by whatever financial means, of land, existing buildings or other im…
Pursuant to articles L. 1222-1 and L. 1222-1-1, the activities other than transfusion activities that may be carried out within blood establishments are as follows: 1° Among the activities related to…
Where the property is put back up for sale by way of a new auction pursuant to the provisions of Article…
…s intended for the personal occupation of the principal, the registry service requests the bulletin n° 2 of the criminal record of the bidder declared the successful bidder and, in the case of a non-t…
Before placing the bids, if the property being seized is a residential property or the business assets of an establishment open to the public and used wholly or partly for accommodation, the lawyer mu…
I.-The tasks of the centres and coordinators mentioned in Article R. 1413-61-3 consist of : 1° Collecting and processing, each in their own field of competence and expertise, alerts relating to each o…
The provisions of this subsection apply to the persons mentioned in III of Article L. 812-2 with the exception of articles R. 814-38 and R. 814-41, including where they have been authorised to continu…
Manufacturers of medicinal products referred to in article R. 5124-2 shall check that the active substances used come from manufacturers, importers or distributors either authorised by the Agence nati…
Manufacturers of medicinal products must be able to document the measures they have taken to ensure that their supplier of excipients complies with good practice under the conditions set out in articl…
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