Article D15-3-2
When, pursuant to article 40-2, the public prosecutor notifies a victim of his decision to discontinue proceedings, he shall inform the victim that he may request a copy of the case file, pursuant to…
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Showing 5861–5870 of 69694 articles for “Art. L 144-2 and Art. R 132-5-3”
When, pursuant to article 40-2, the public prosecutor notifies a victim of his decision to discontinue proceedings, he shall inform the victim that he may request a copy of the case file, pursuant to…
For the application of this book to Saint-Barthélemy: 1° The references to the Prefect are replaced by the reference to the Representative of the State in Saint-Barthélemy; 2° In Article R. 810-1, the…
For the application of this book in Saint-Martin: 1° References to the Prefect are replaced by references to the State representative in Saint-Martin; 2° In Article R. 810-1, the reference to Article…
The general rapporteur may call on external rapporteurs chosen from among the members of the Conseil d'Etat, magistrates, category A civil servants or contractual State employees of equivalent level w…
The court shall rule within a period of one month from the date of referral, after having notified all interested parties fifteen days in advance by delivery against receipt or by registered letter wi…
The decision of the judicial court may be the subject of an appeal to the Court of Cassation lodged, investigated and judged under the conditions provided for by the Code of Civil Procedure in matters…
For the application of the regulatory provisions of Book I in the Wallis and Futuna Islands:1° In Article R. 2111-9:a) 2° is deleted;b) In 5°, the words: "other technical standards drawn up by Europea…
Where a signature is required, the use of an advanced electronic signature based on a qualified certificate is required under the conditions set out in Regulation (EU) No 910/2014 of 23 July 2014 on e…
Any person who sterilizes with a view to placing on the market CE-marked medical devices designed by their manufacturer to be sterilized before use or systems or kits referred to in Section 10 of this…
As part of the procedure applicable to custom-made medical devices, the manufacturer must draw up documentation including the name and address of the manufacturer, the place or places of manufacture,…
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