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Showing 1891–1900 of 48358 articles for “Art. 6 §2”
The EC quality assurance system for production with surveillance is the procedure whereby a manufacturer: 1° has a quality assurance system approved by a notified body of his choice ; 2° entrusts this…
In order to assess the quality assurance system, the notified body shall carry out all necessary objective assessments of the elements of this system. In particular, it shall ensure that the system gu…
…rsonal protective equipment envisaged, including the technical file provided for in Article R. 4313-6 relating to the model for which an EC type-examination certificate has been issued; 2° Documentati…
In order to be approved, the EC production quality assurance system proposed by the manufacturer must guarantee that each item of personal protective equipment subject to this procedure conforms to th…
The documentation on the quality assurance system shall include in particular a description of: 1° the quality objectives, the organization chart and the distribution of responsibilities within the ma…
The notified body chosen by the manufacturer to assess the quality assurance system shall carry out the necessary checks to determine whether this system is such as to ensure conformity of production…
…nd decide whether the quality assurance system continues to meet the provisions of Articles R. 4313-64 to R. 4313-67. The body must notify the manufacturer of its decision concerning the modified qual…
The notified body checks, by means of surveillance, that the manufacturer duly fulfils the obligations arising out of the approved quality assurance system.
…ived and to the results of the individual dosimetric monitoring referred to in I of Article R. 4451-65. II -When the radiation protection advisor finds that one of the doses estimated as part of the p…
Workers have access to all the results of their individual dosimetric monitoring and to their effective dose. They may ask the occupational physician or the Institut de Radioprotection et de Sûreté Nu…
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