Article L2141-13
The detailed rules for the application of this chapter are determined by decree in the Conseil d'Etat, and in particular : 1° The procedures for applying Article L. 2141-6 and in particular the activi…
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Showing 7441–7450 of 13025 articles for “Art. Euronext Harmonised Market Rules — derivatives”
The detailed rules for the application of this chapter are determined by decree in the Conseil d'Etat, and in particular : 1° The procedures for applying Article L. 2141-6 and in particular the activi…
The president of the court or the magistrate delegated for this purpose shall rule urgently by order, in the light of the decision and any other useful documents. However, he shall have the option of…
The request by the chairman of the board of directors or the management board of the société anonyme à participation ouvrière is made at least three months before the date of the extraordinary general…
The Observatory adopts its rules of procedure by an absolute majority of its members. These rules shall stipulate the frequency of meetings, which may not be less than two per year. The Observatory is…
…ting or reverses the rejection thereof may, if the date set for the leave has passed when he or she rules on the appeal, decide on another date or decide that a new date will be set by the enforcement…
I.-This article applies to the agreement mentioned in I of article L. 441-3 when it relates to mass-market products defined as non-durable products that are consumed frequently and repeatedly. The lis…
…s party to the Agreement on the European Economic Area, as well as from the European Securities and Markets Authority when these requests relate to the implementation of Directive 2011/61/EU of the Eu…
I.-Placing on the market or putting into service on French territory a medical device or its accessories is punishable by five years' imprisonment and a fine of 375,000 euros: 1° Without the EU declar…
…of 29 June 2016 supplementing Directive 2014/65/EU of the European Parliament and of the Council on markets in financial instruments by technical regulatory standards specifying information to be noti…
In order to obtain a marketing authorisation in France and in at least one other Member State of the European Union, for a veterinary medicinal product which does not have any authorisation in the Eur…
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