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Showing 4301–4310 of 18481 articles for “Art. CE 5-5-2010 n° 301419”
The manufacturer undertakes to fulfil all the conditions necessary for the approved quality system to remain effective.
The manufacturer must keep at the disposal of the national authorities, for a period of ten years from the last date of manufacture, the elements to be transmitted with any application for assessment…
A decision by the Regional Director of Business, Competition, Consumer Affairs, Labour and Employment will be deemed to have been rejected if the competent Minister to whom the matter is referred rema…
The "EC quality assurance system" is the procedure whereby a notified body certifies that the manufacturer has taken all necessary measures to ensure that the manufacturing process, including final in…
…shall take an adequate sample of the personal protective equipment at random intervals, at least once a year. Under its responsibility, it shall examine the sample and perform the appropriate tests d…
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…
…onal protective equipment examined do not conform to the model described in the EC type-examination certificate and the applicable technical rules, the notified body shall take the appropriate measure…
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