Article L421-6
…with regard to the risks and categories of risk covered by the standards applicable to it, where it complies with non-mandatory national standards transposing European standards, the references of whi…
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Showing 2951–2960 of 13796 articles for “Art. European Commission report COM”
…with regard to the risks and categories of risk covered by the standards applicable to it, where it complies with non-mandatory national standards transposing European standards, the references of whi…
In the context of the administrative cooperation organised by Regulation (EU) 2017/2394 of the European Parliament and of the Council of 12 December 2017 on cooperation between national authorities re…
The results of investigations and inspections are set out in a written report. This report shall indicate, in particular, any facts that may constitute breaches of European regulations, of this Code,…
…General of the Regional Health Agency may, subject to the rights of third parties, make public the reports relating to the expert opinions which he has commissioned.
…ntracting entities, concession contracts concluded by contracting entities in a Member State of the European Union or in a specific geographical area of a Member State are subject to the rules set out…
…he detailed rules for applying this article are laid down by decree in the Conseil d'Etat after the European Commission has declared the obligation laid down in this article to be compatible with Euro…
…2324-2 to R. 2324-4, the purchaser shall publish a contract notice in the Official Journal of the European Union drawn up in accordance with the model set out in the European Commission Regulation e…
The Commission makes the updated list of mediators available to the public on its website and provides the link to the European Commission's website dedicated to consumer mediation as well as the link…
…vatives and cells from the human body, whatever their level of processing, in a Member State of the European Union or a party to the Agreement on the European Economic Area. These same establishments…
Manufacturers of in vitro diagnostic medical devices may import or export tissues, their derivatives and cells from the human body, whatever their level of processing, when these products are intended…
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