Article R5211-22
In order to comply with the essential requirements relating to design and manufacture, medical devices, other than active implantable devices, must be designed, manufactured and packaged in such a way…
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Showing 561–570 of 62249 articles for “Art. R. 223-20 and R. 223-22”
In order to comply with the essential requirements relating to design and manufacture, medical devices, other than active implantable devices, must be designed, manufactured and packaged in such a way…
Recourse to the option mentioned in article R. 2372-19 must be indicated in the consultation documents. The proportion of supplies or services that may be acquired during performance without having be…
…contract holder is a small or medium-sized enterprise or a craftsman within the meaning of article R. 2151-13, a cooperative production company, an agricultural producers' group, a craftsmen's cooper…
…y or sole trader who ceases to fulfil the conditions or respect the obligations mentioned in 4°, 5° and 6° of article R. 7232-17 or who repeatedly fails to respect the obligations defined in article R…
…the commercial authorisation lapses within three years of the notification provided for in Article R. 752-19 or, where applicable, to article R. 752-39 : 1° For sales areas that have not been opened…
…er single or repeated exposure, pursuant to Regulation (EC) No 1272/2008 of the European Parliament and of the Council of 16 December 2008 on classification, labelling and packaging of substances and…
The opinion issued by the Social and Economic Committee as part of the consultation carried out in application of article L. 2421-3 is expressed by secret ballot after hearing the interested party.
In the light of the investigation file and the opinions expressed, the Prefect entrusts the Director General of the Regional Health Agency with drawing up a summary report on the request and the resul…
…may, by reasoned decision, refuse to include a medicinal product on the list referred to in Article R. 5121-202 for any public health reason, in particular when the benefit/risk balance of the medicin…
The programme is run by an operator, chosen and contracted for this purpose by the company marketing the medicinal product. The operator is chosen on the basis of the guarantees of independence that i…
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