Article R214-10
I.- Referral to the mediator shall be made by letter delivered against a signature or by any other means capable of establishing proof of the date of referral and shall include: 1° If the applicant is…
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Showing 9481–9490 of 9873 articles for “Art. BOI-RFPI-BASE-30-20 n° 260”
I.- Referral to the mediator shall be made by letter delivered against a signature or by any other means capable of establishing proof of the date of referral and shall include: 1° If the applicant is…
The medical report referred to in article R. 425-11 is drawn up by an Office français de l'immigration et de l'intégration doctor on the basis of a medical certificate drawn up by the doctor who usual…
The register of intermediaries referred to in Article R. 512-6 includes the following information:1° The intermediary's registration number ;2° In the case of a natural person, his identity, the addre…
The authorised and sworn fraud prevention officers referred to in Article L. 5312-13-1 have a right of communication which enables them to obtain, without being prevented by professional secrecy, the…
When it is consulted pursuant to IV of article L. 1611-10, the Consultative Commission on the Financial Responsibility of Local Authorities shall give its opinion within three months of the date of re…
A. - The report provided for in Article L. 2312-1 includes the following information: 1° The budgetary guidelines envisaged by the municipality relating to forecast changes in expenditure and revenue,…
The professional practice standard relating to the selection of items to be audited, approved by the Minister of Justice, is set out below:PROFESSIONAL PRACTICE STANDARD RELATING TO THE SELECTION OF I…
The professional practice standard relating to obtaining an understanding of and making use of the work of the internal audit, approved by the Minister of Justice, is set out below: PROFESSIONAL PRACT…
I.-This article applies to the post-authorisation studies referred to in article R. 5121-178 which are carried out by the holder of the authorisation referred to in article L. 5121-8 in order to compl…
I.-Any company or organisation exploiting a medicinal product or a product mentioned in article R. 5121-150 is required to transmit electronically to the European Medicines Agency a periodic safety up…
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