Article L7313-6
…ain such a prohibition, it shall contain, unless the parties expressly agree otherwise, a statement of the companies or products that the traveller, sales representative or sales agent already represe…
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Showing 4891–4900 of 58474 articles for “Art. 17 January 2020 · Law 89-462 of 6 July 1989”
…ain such a prohibition, it shall contain, unless the parties expressly agree otherwise, a statement of the companies or products that the traveller, sales representative or sales agent already represe…
…the procedure whereby a manufacturer: 1° has a quality assurance system approved by a notified body of his choice ; 2° entrusts this body with the task of checking, by means of surveillance, that it c…
…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 guarantees the confor…
The display, offering for sale, sale, hire, import, transfer or making available for any purpose whatsoever of new machinery or personal protective equipment or equipment considered to be new subject…
…e EC production quality assurance system proposed by the manufacturer must guarantee that each item of personal protective equipment subject to this procedure conforms to the model which was the subje…
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…
…all carry out the necessary checks to determine whether this system is such as to ensure conformity of production with the applicable technical rules. Such conformity is presumed when the manufacturer…
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.
The removal of tissues and cells and the collection of human body products from a person who has been duly declared dead may only be carried out for therapeutic or scientific purposes and under the co…
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