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Showing 1691–1700 of 48367 articles for “Art. 494-6 al. 2”
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…
…ies within the manufacturer in the fields relating to the quality of personal protective equipment; 2° the examinations, inspections and tests to be carried out by the manufacturer; 3° the means inten…
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…
The manufacturer must inform the body which approved his quality assurance system of any proposed changes to that system. The body must examine the proposed modifications and decide whether the qualit…
The notified body checks, by means of surveillance, that the manufacturer duly fulfils the obligations arising out of the approved quality assurance system.
…r, as the case may be, the person in charge of the competent radiation protection body mentioned in 2° of Article R. 4451-112, shall ensure the confidentiality of the personal data mentioned in I and…
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…
…for whom he is responsible for the enhanced individual monitoring provided for in Article R. 4451-82. II.-As part of the enhanced individual monitoring provided for in article R. 4451-82, the occupat…
The social and economic committee of the user undertaking shall, if it considers it necessary, instruct one or more of its members belonging to the staff delegation to take part in inspections and per…
An occupational physician may not be assigned exclusively to the sector reserved for temporary workers. A derogation may be granted by the Regional Director of Companies, Competition, Consumption, Lab…
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