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Showing 1231–1240 of 13025 articles for “Art. Euronext Harmonised Market Rules — derivatives”
Within two months of the date on which the dossier is deemed to be complete, the Minister for Research and, where applicable, the Director General of the Regional Health Agency may, in the cases provi…
The declaration is made up of a letter signed by the legal representative of the applicant organisation and a supporting file, entered using a teleservice. The letter describes the activity and certif…
Any change in the information contained in the declaration file that is likely to result in a substantial change in the conditions under which the declared activities are carried out, in particular a…
The dossier is deemed to be complete if, within one month of receipt, the Minister responsible for research or, where applicable, the Director General of the regional health agency, has not informed t…
Within the scope of the declaration, organisations must be able to provide the following information at any time: 1° The nature and number of samples held; 2° The characteristics of the samples held;…
…hibition decision may include requirements relating to the preservation of tissues, cells and their derivatives; it may organise their transfer to another organisation or order their destruction.
A grouping of orders may be formed with purchasers from other Member States of the European Union, provided that this choice has not been made with the aim of evading the application of national provi…
…al cooperation, the statutes or a decision of the competent body of this entity shall determine the rules applicable to the contracts of this entity, which shall be:1° Either the law of the State in w…
The works, supplies or services to be provided under the public contract are defined by reference to technical specifications.
The agreement setting up the consortium, signed by its members, defines the operating rules of the consortium. It may entrust one or more of its members with the task of carrying out all or part of th…
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