Article L823-3-1
I. - Where a public interest entity appoints a single auditor, the single auditor may not certify the accounts of the public interest entity for a period exceeding ten years.However, at the end of tha…
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Showing 411–420 of 65302 articles for “Art. L 441-3-1”
I. - Where a public interest entity appoints a single auditor, the single auditor may not certify the accounts of the public interest entity for a period exceeding ten years.However, at the end of tha…
Where the regulations provide for a procedure involving the sampling of one unit of a model and then, in the event of non-compliance, additional units of the same model, these additional units may be…
When they are entered on the supplementary electoral roll for the municipality drawn up pursuant to article LO 227-2 of the Electoral Code, nationals of a Member State of the European Union other than…
The Autorité des marchés financiers may only be held liable for the application of the provisions of Regulation (EU) 2017/1129 and its delegated regulations in respect of the approval of prospectuses.
…of the redemption of units or shares or the issue of new units or shares of an AIF when exceptional circumstances so require and if the interests of unitholders, shareholders or the public so dictat…
In establishments open to the public with a capacity of more than two hundred people, the employer must provide training for professionals in contact with users and customers on how to welcome and sup…
…earing the words "Etudiant des métiers" by the organisation providing their training. This card enables the apprentice to demonstrate to third parties throughout the country the specific nature of the…
The duration of the professional transition project corresponds to the duration of the training course.
Any holder of a marketing authorisation for a medicinal product or any operator of such a medicinal product is required, within one year of the promulgation of Act 2011-2012 of 29 December 2011 on rei…
When carrying out their activity on national territory, the qualified person in pharmacovigilance referred to in paragraph 8 of Article 77 of Regulation (EU) 2019/6 of 11 December 2018 shall have prof…
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