Article R2135-26
Appropriations that have not been committed by a beneficiary organisation during the financial year are returned to the fund and added to the total amount of appropriations of the same type that may b…
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Showing 3771–3780 of 12461 articles for “Art. legal committee”
Appropriations that have not been committed by a beneficiary organisation during the financial year are returned to the fund and added to the total amount of appropriations of the same type that may b…
Commercial court clerks may be appointed by order of the Garde des Sceaux, Minister of Justice:1° Persons registered on the aptitude list provided for in Article R. 742-16 ;2° Persons who, having pass…
I. - The articles R. 5721-1 and R. 5721-2 are applicable in French Polynesia subject to the adaptations provided for in II and III.II. - For the application of Article R. 5721-1, the words: "of the Ge…
I.-Article R. 5722-1 is applicable in French Polynesia subject to the adaptations provided for in II. II.-For the application of Article R. 5722-1, the words: "The provisions of Book III of Part Two"…
The enactment of the deliberations of the Territorial Council and the deliberations of the Executive Council taken by delegation, as well as the acts of the President of the Territorial Council, of a…
The enactments of the deliberations of the Territorial Council and the deliberations of the Executive Council taken by delegation, as well as the acts of the President of the Territorial Council, of a…
For medical devices other than those subject to clinical investigations, the certification procedures mentioned in Article R. 5211-14 are as follows: 1° The EC declaration of conformity ; 2° The EC de…
For medical devices to be subject to clinical investigations, the manufacturer must comply with the provisions of Title II of Book I of Part I of this Code.
For the purposes of placing a custom-made medical device on the market, the manufacturer shall follow the procedure defined in Article R. 5211-51. The Director General of the Agence nationale de sécur…
In the case of active implantable medical devices or medical devices in Class III or Class II b, the manufacturer shall take all necessary measures to ensure that the manufacturing process guarantees…
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