Article R1413-4
The term of office of the members of the Board of Directors is four years, with the exception of the members mentioned in 1° bis of article R. 1413-3. For the latter, the term of office of deputies en…
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Showing 6141–6150 of 7044 articles for “Art. Règlement”
The term of office of the members of the Board of Directors is four years, with the exception of the members mentioned in 1° bis of article R. 1413-3. For the latter, the term of office of deputies en…
The couple or unmarried woman who wishes to offer their embryos for reception must give their written consent, in application of article L. 2141-5, after at least one interview with the multidisciplin…
I.-Persons who set up or manage an approved establishment in accordance with the procedure set out in article R. 2311-2 may receive financial assistance from the State. This assistance is paid under c…
I.-The authorisation issued by the President of the Departmental Council indicates: 1° The name and company name of the legal entity managing the establishment or service; 2° The type of establishment…
A public interest entity that applies to the bureau of the High Council for authorisation to extend the term of office of its statutory auditor, pursuant to III of article L. 823-3-1, shall send him a…
The Local Finance Committee of French Polynesia deliberates validly when fifteen members with voting rights are present.If, after the first notice, the Committee has not met in sufficient number, a ne…
The Conseil national de l'ordre acknowledges receipt of the application for authorisation to practise as a midwife submitted by a person holding evidence of formal qualifications as a midwife obtained…
The Agence nationale pour l'amélioration des conditions de travail may set up regional offices. Each regional directorate is supported by a regional joint body which participates, in collaboration wit…
The application for authorisation referred to in article R. 5122-2 sent by electronic means is drawn up on a site accessible online, via the Internet network, offering the functionalities necessary fo…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 is required to: 1° Record all adverse reactions suspected of being due to a medicinal product o…
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