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Showing 3321–3330 of 64913 articles for “Art. R 315-5 and Art. R 315-7 s.”
The manufacturer undertakes to fulfil all the conditions necessary for the approved quality system to remain effective.
The notified body checks, by means of surveillance, that the manufacturer duly fulfils the obligations arising out of the approved quality assurance system.
The manufacturer must allow the notified body access to the locations of design, manufacture, inspection, testing and storage and must provide all necessary information, in particular: 1° the document…
If the body considers that the conditions necessary for approval of the quality system are no longer fulfilled, it will withdraw this approval. This withdrawal prohibits the placing on the market of t…
The notified body carries out periodic audits to ensure that the manufacturer maintains and applies the approved quality system. It provides the manufacturer with an audit report. The frequency of the…
The notified body makes unannounced visits to the manufacturer, the need for and frequency of which are determined on the basis of the control system managed by the body. The criteria for choosing the…
When, for a building or civil engineering operation involving several companies and not belonging to the first or second category, it is planned to carry out work presenting particular risks included…
When, during a third category operation, a coordinator becomes aware, after the work has begun, of the existence of one or more works presenting particular risks included on the list established by th…
By way of derogation from the provisions of sub-sections 1 and 2 of section 2 of Chapter IV of Title II of Book VI of Part Four of this Code, the information and prevention visit or the pre-recruitmen…
Referral to the committee for conciliation is an obligatory prerequisite to any contentious appeal, when the dispute arises from a decision, whether or not subject to internal appeal, taken by a feder…
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