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Showing 3011–3020 of 50982 articles for “Art. 387-3 to 387-6”
…s that the traveller, sales representative or sales agent already represents and an undertaking not to take on any new representation during the term of the contract without the employer's prior autho…
…atives are elected in accordance with the procedures laid down by the departmental council pursuant to Article L. 1424-24-2.
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…
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…
…ation chart and the distribution of responsibilities within the manufacturer in the fields relating to the quality of personal protective equipment; 2° the examinations, inspections and tests to be ca…
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…
…nufacturer 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 quality assu…
The notified body checks, by means of surveillance, that the manufacturer duly fulfils the obligations arising out of the approved quality assurance system.
Any person who fits sick or disabled people with custom-made orthotic or orthopaedic appliances or mass-produced orthotic or orthopaedic appliances is considered to be practising the profession of ort…
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