Article R322-2
Undertakings subject to State supervision under article L. 310-1 may have no other object than to carry out the operations mentioned in article R. 321-1, and those directly arising therefrom, to the e…
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Showing 3051–3060 of 53949 articles for “Art. R 224-2”
Undertakings subject to State supervision under article L. 310-1 may have no other object than to carry out the operations mentioned in article R. 321-1, and those directly arising therefrom, to the e…
The application for approval, accompanied by a file drawn up in accordance with article R. 329-1, is sent by registered letter with acknowledgement of receipt to the Minister for Culture, who issues a…
The supervisory authorities of the territorial or, where applicable, regional chambers of commerce and industry participating in the grouping check that the representatives have been appointed in acco…
The chairman of the board of directors of the guarantee fund shall inform the public prosecutor at the court of appeal in whose jurisdiction the interested party has his professional domicile, the gov…
Subject to the provisions of articles L. 6152-4, L. 6154-4 and R. 6152-30 as well as those ofarticle 9 of decree no. 91-966 of 20 September 1991 relating to associated staff in hospital and university…
For the application of the provisions of sub-sections 1 to 3, the following are not considered to be sub-contractors: 1° Members of the same grouping in relation to each other; 2° Economic operators o…
The time limits for receipt of tenders submitted under a formalised procedure may not be less than the minimum time limits specific to each procedure, as defined in Chapter I of Title VI. Where certai…
In the two forms of grouping mentioned in article R. 2142-20, one of the economic operators who is a member of the grouping, designated in the application and in the tender as the lead contractor, rep…
Manufacturers of medical devices and the companies and organisations operating these devices shall, at the reasoned request of the Director of the Agence nationale de sécurité du médicament et des pro…
In order to comply with the essential requirements relating to design and manufacture, active implantable medical devices must be designed, manufactured and packaged in such a way as to meet the follo…
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