Article R5211-32
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.
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Showing 1271–1280 of 69003 articles for “Art. L 221-32 and Art. D 221-111-1”
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.
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If the challenge is accepted, the conciliator shall be replaced without delay.
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When a general renewal of the industrial tribunals makes it impossible to refer a case that was the subject of a tie vote prior to this renewal, the case is taken up again, as the case may be, before…
The application submitted by an association shall include in particular: 1° A copy of the Journal officiel publishing the declaration of the association or, as regards the departments of Bas-Rhin, Hau…
Nurses are personally responsible for their decisions and the professional acts they are authorised to perform. They must not practise their profession in conditions that could compromise their indepe…
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