Article R4311-89
In addition to its Chairman, the Disciplinary Chamber of First Instance shall comprise :1° Where the total number of nurses on the most recently published roll is less than or equal to 10,000, six ful…
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Showing 7051–7060 of 38200 articles for “Art. R 210-6”
In addition to its Chairman, the Disciplinary Chamber of First Instance shall comprise :1° Where the total number of nurses on the most recently published roll is less than or equal to 10,000, six ful…
The date of the elections to the Disciplinary Chamber of First Instance is announced by the National Council under the same conditions as those laid down in article R. 4311-58.Candidates shall make th…
Any person who sterilizes with a view to placing on the market CE-marked medical devices designed by their manufacturer to be sterilized before use or systems or kits referred to in Section 10 of this…
As part of the EC declaration of conformity procedure, production quality assurance, the manufacturer shall submit to an authorised body for verification the quality system which he has set up for the…
Within the framework of the EC declaration of conformity procedure, product quality assurance, for class II a medical devices or class I medical devices, the provisions laid down in Article R. 5211-49…
As part of the EC declaration of conformity procedure, production quality assurance, for active implantable medical devices or medical devices in class IIb or class III, the manufacturer submits an ap…
As part of the EC declaration of conformity procedure, product quality assurance, the manufacturer shall submit to an authorised body for verification the quality system which he has set up for the fi…
As part of the procedure applicable to custom-made medical devices, the manufacturer must draw up documentation including the name and address of the manufacturer, the place or places of manufacture,…
For Class IIa medical devices or Class I medical devices, the provisions of Article R. 5211-46 apply subject to the following modifications: 1° For class II a medical devices, the authorised body veri…
As part of the procedure for the EC declaration of conformity, a full quality assurance system, the manufacturer must submit to an approved body for verification the quality system which he has set up…
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