Article R6323-15
If the regional cross-industry joint committee rejects all or part of a request for reimbursement, it will notify the employee of the reasons for the rejection by any means that provides a date certai…
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Showing 6721–6730 of 59430 articles for “Art. Cass. 1ère civ. 5-1-2023”
If the regional cross-industry joint committee rejects all or part of a request for reimbursement, it will notify the employee of the reasons for the rejection by any means that provides a date certai…
The administrative authority defined in article R. 7124-1 grants the authorisation, for a renewable period of one year, on the assent of a commission whose composition and mode of operation are determ…
The information provided for in the last paragraph of article L. 7124-1-5 is delivered by any means to the child's legal representatives by the administrative authority defined in article R. 7124-1.
The decision to suspend approval must be justified by the urgency of the situation and can only be based on facts that immediately and seriously jeopardise the health or morals of the child. Reasons m…
Approval, or renewal of approval, may only be granted when the child's physical and psychological safety is sufficiently guaranteed. As part of the examination of the application, the administrative a…
Foreign nationals who come to France for one of the following reasons are considered as trainees for the purposes of obtaining a temporary residence permit bearing the word "stagiaire" (trainee) as pr…
The articles L. 5212-27, L. 5212-29 to L. 5212-32 are applicable in French Polynesia.
At the end of each financial year, the Prefect draws up, for each municipality and on the basis of the information collected, an annualised balance sheet of all the operations carried out, which summa…
Article D. 2215-1 is applicable in French Polynesia subject to the following adaptation: after the words: "of Book I of the Internal Security Code", the words: "in the version applicable in French Pol…
Where an application for marketing authorisation in France is made for a medicinal product which has already been authorised or is the subject of an application for marketing authorisation currently b…
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