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Showing 5271–5280 of 40190 articles for “Art. Cass. 3e civ. 4-6-1971”
On pain of nullity, requisitions relating to technical data making it possible to identify the source of the connection or data relating to the terminal equipment used mentioned in 3° of II bis of art…
In addition to the other penalties provided for in this Code, the following shall be confiscated 1° goods that have been or had to be substituted in the cases provided for in articles 411-2 a, 417-2 c…
The possession, control, management and dispensing of medicines strictly related to the harm reduction mission for drug users, the list of which is set by order of the Minister for Health, are carried…
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…
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…
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…
As part of the procedure for the EC declaration of conformity, product quality assurance, for class II b medical devices, the manufacturer must submit an application to the authorized body for assessm…
The decision that the summons has lapsed may be rescinded, in the event of error, by the judge who issued it.
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