Article L211-18
…e date and in accordance with the conditions defined in the General Regulations of the Autorité des marchés financiers or, failing this, by an agreement between the parties, automatically discharges t…
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Showing 5411–5420 of 23566 articles for “Art. Cass. com. 11 March 2003”
…e date and in accordance with the conditions defined in the General Regulations of the Autorité des marchés financiers or, failing this, by an agreement between the parties, automatically discharges t…
The purchaser shall guarantee economic operators and works, supplies and services from States which are parties to the Agreement on Government Procurement concluded within the framework of the World T…
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…
…ld by the company, or in the bearer share accounts held by an intermediary mentioned in Article L. 211-3 of the Monetary and Financial Code, or, where applicable, in a shared electronic recording devi…
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…
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