Article R6223-82
The competent council of the ordre des médecins or the ordre des pharmaciens decides on the application for registration under the conditions set out in articles L. 4112-3 and L. 4112-4 and articles L…
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Showing 2801–2810 of 52053 articles for “Art. II-5°”
The competent council of the ordre des médecins or the ordre des pharmaciens decides on the application for registration under the conditions set out in articles L. 4112-3 and L. 4112-4 and articles L…
Articles R. 6223-79 to R. 6223-83 are applicable in the event of the formation of private equity companies for the liberal professions of medical biologists by way of merger, demerger or universal tra…
The application for registration shall be sent by a joint representative appointed, in the articles or in a separate deed, by the members of the company, to the council of the competent Bar or Bars wi…
A société de participations financières de profession libérale de biologistes médicaux is formed subject to the suspensive condition of its registration on the roll of the Order of Physicians, when at…
Natural or legal persons practising the profession of medical biologist may, under the conditions laid down inarticle 31-1 of law no. 90-1258 of 31 December 1990, set up a "société de participations f…
I.- Subject to the provisions of II, the provisions of the articles mentioned in the left-hand column of the following table shall apply in New Caledonia, in the wording indicated in the right-hand co…
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…
In order to comply with the essential requirements relating to design and manufacture, medical devices, other than active implantable devices, must be designed, manufactured and packaged in such a way…
Before applying for the issue of the EC design examination certificate or EC type examination certificate referred to in Articles R. 5211-40 and R. 5211-41 respectively, manufacturers of medical devic…
The manufacturer is required to update the risk analysis and management system referred to in Article R. 5211-23-2 by analysing all elements relating to the medical devices he manufactures and taking…
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