Article 576
The declaration of appeal must be made to the registrar of the court which handed down the contested decision.It must be signed by the registrar and by the applicant for judicial review himself or by…
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Showing 5261–5270 of 64636 articles for “Art. CE 12-5-2022 n° 416727 and CE 27-3-2020 n° 428234”
The declaration of appeal must be made to the registrar of the court which handed down the contested decision.It must be signed by the registrar and by the applicant for judicial review himself or by…
Pursuant to article L. 3114-9, the proportion of services or works that the tenderer must entrust to small and medium-sized enterprises or third parties may not be less than 10% of the total estimated…
…ly a branch agreement or a professional agreement on employment which provides for this possibility and determines the procedures for its direct application. The aid is granted on the advice of the so…
Where the commercial activity within the jurisdiction of a court has ceased altogether as a result of its transfer to the jurisdiction of another court, the deregistration shall be effected automatica…
The person concerned, of French nationality and residing abroad, who is unable to fulfil the obligations resulting from article 706-25-7 because of the absence of French representation in the foreign…
Live performance promoters who are nationals of a European country may establish themselves in order to carry out their activities in France without having to declare their activity, provided that the…
…lts in his death, the employer shall inform the Labour Inspectorate official responsible for the place where the accident occurred immediately and at the latest within twelve hours of the worker's dea…
…rnalists treated as such, within the meaning of articles L. 7111-3 to L. 7111-5 of the Labour Code, and other authors of works included in the press publications referred to in Article L. 218-1 of thi…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé or the applicant for marketing authorisation may refer the matter to the European Medicines Agency with…
…rest to the European Union, the Director General of the National Agency for the Safety of Medicines and Health Products or the applicant shall refer the matter to the European Medicines Agency for app…
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