Article R2132-2
The consultation documents are made available to economic operators free of charge. For contracts that meet a need whose estimated value is equal to or greater than €40,000 excluding tax and whose pro…
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Showing 3641–3650 of 21427 articles for “Art. Cass. com. 31 March 2004”
The consultation documents are made available to economic operators free of charge. For contracts that meet a need whose estimated value is equal to or greater than €40,000 excluding tax and whose pro…
Once the loan has been concluded, the creditor shall regularly warn the borrower, on paper or on another durable medium, at least when the value of the total outstanding amount payable by the borrower…
The written questions referred to in the third paragraph of Article L. 225-108 are sent to the registered office by registered letter with acknowledgement of receipt addressed to the Chairman of the B…
I. - A UCITS with a formula is a UCITS which meets the following two conditions:1° It is managed passively and its management objective is to reach, at the end of a given period, an amount determined…
…en down into the following aggregate categories, according to the types defined by the Autorité des marchés financiers: 1° Entrance and exit fees ; 2° Recurring management and operating expenses, incl…
I.-The counterparty risk on a single counterparty is the risk that the counterparty will default on one of its obligations, resulting in a financial loss for the société civile de placement immobilier…
The register of hybrid groups shows the proprietary medicinal products included in each hybrid group. The hybrid groups are grouped by active substance designated by its common name preceded by the wo…
When a medicinal product is the subject of a reassessment of the risk-benefit balance, the Director General of the Agence nationale de sécurité du médicament et des produits de santé shall inform the…
As part of the EC declaration of conformity procedure, product quality assurance, the manufacturer shall submit to an authorised body for verification the quality system which he has set up for the fi…
For Class IIa devices, the authorized body must, as part of the assessment of the quality system, assess the technical documentation for at least one representative sample of each device subcategory i…
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