Article D47-1-36
The Financial Public Prosecutor referred to in Article 705 and the public prosecutors with territorial jurisdiction in the inter-regional courts specialising in economic and financial matters provided…
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Showing 471–480 of 36767 articles for “Art. L 581-36”
The Financial Public Prosecutor referred to in Article 705 and the public prosecutors with territorial jurisdiction in the inter-regional courts specialising in economic and financial matters provided…
The official receiver shall rule on the sale after having heard the observations of the auditors and heard or duly summoned the debtor and his spouse where the latter is in one of the situations provi…
Where a party is represented by a lawyer or by a lawyer at the Conseil d'Etat and the Cour de cassation, the procedural acts, with the exception of the notification of the decision provided for in art…
The Commission of Nurses for the region designated by order of the Minister for Health comprises :1° The Regional Director for Youth, Sport and Social Cohesion or his/her representative, as Chairman ;…
The regional directorate for youth, sport and social cohesion provides the committee's secretariat.
The use of electronic Internet voting is organised in compliance with the fundamental principles governing electoral operations, access to the vote for all voters, the secrecy of the ballot, the free…
The marketing authorisation may impose one or more of the following conditions, which must be mentioned in the risk management system: 1° The implementation of measures to ensure the safe use of the m…
The Director General of the Autorité des relations sociales des plateformes d'emploi shall publish on the website referred to in Article R. 7343-10 , on a date set by order of the Minister for Employm…
The clinical evaluation and its results are included or duly referenced in the technical documentation for the device referred to in Article R. 5211-39. The clinical evaluation and its documentation a…
Implantable medical devices, active implantable medical devices and class III devices must be subject to clinical investigations, unless the use of existing clinical data can be duly justified.
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