Article 125-0 A
I. - 1° The products attached to capitalisation bonds or contracts as well as to investments of the same nature subscribed with insurance companies established in France are, when the bond, contract o…
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Showing 9031–9040 of 64732 articles for “Art. I-1°-d”
I. - 1° The products attached to capitalisation bonds or contracts as well as to investments of the same nature subscribed with insurance companies established in France are, when the bond, contract o…
The declaration mentioned in I of article L. 1262-2-1 is appended to the single personnel register of the company hosting the seconded employees.
The staff of the departments of the High Council is composed in accordance with Article 16 of Law No. 2017-55 of 20 January 2017 on the general statute of independent administrative authorities and in…
The employer shall record, in an appendix to the single document: 1° Collective data useful for assessing individual exposure to the risk factors mentioned in Article L. 4161-1 in order to facilitate…
Subject to the adaptations provided for in this chapter, the following provisions of this code shall apply in the Wallis and Futuna Islands:1° Books I to III, with the exception of the fourth paragrap…
Financial investment advisers must:1° Act honestly, loyally and professionally, in the best interests of their clients;2° Exercise their activity, within the limits authorised by their status, with du…
The written test of the examination with option in civil matters, lasting five hours, has as its object the processing of a file relating to one of the missions likely to be entrusted to a judicial ad…
The publication of decisions, acts and documents provided for in the Official Bulletin of Industrial Property distributed in electronic form, under conditions such as to guarantee its authenticity, pr…
The applicant for marketing authorisation is responsible for the accuracy and sincerity of the information and data provided to the Agence nationale de sécurité sanitaire de l'alimentation, de l'envir…
Where a veterinary medicinal product, which has already been authorised or is the subject of an application for marketing authorisation under examination in another Member State of the European Union,…
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