Article R4722-16
The labour inspector may ask the employer to have noise exposure measured by a body accredited in this field, in order to ensure compliance with the obligations relating to the prevention of the risks…
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Showing 771–780 of 62896 articles for “Art. II · Arts. R 611-13 to R 611-16”
The labour inspector may ask the employer to have noise exposure measured by a body accredited in this field, in order to ensure compliance with the obligations relating to the prevention of the risks…
The contracting authority shall indicate in the consultation documents the minimum requirements with which tenders must comply.
Purchase orders are written documents sent to the holders of the framework agreement, specifying the services described in the framework agreement that are to be carried out and specifying the quantit…
For the application of the provisions of Article R. 612-26 of the Monetary and Financial Code, the information and documents relating to the situation of the said undertakings must be made available t…
For the application of article R. 1336-4 in Mayotte, the references to articles L. 4111-1 and L. 4111-3 of the Labour Code are replaced by the reference to article L. 233-1 of the Mayotte Labour Code.
Before any decision on suspension or withdrawal is taken, the person concerned shall be given the opportunity to submit written or oral observations.Where the application for suspension or withdrawal…
Within the same eight-day period, extracts from the minutes are brought to the attention of the public by means of posters affixed for one month to the door of the town hall, as well as to the door of…
The entries relating to the decisions referred to in Article R. 123-122 when:1° Safeguard proceedings have been terminated pursuant to Article L. 622-12 ;2° Reorganisation proceedings have been termin…
Declarations concerning the registration of commercial agents, changes to their situation or the cessation of their activity shall be made electronically. For all the electronic transmissions referred…
In order to comply with the requirements relating to design and manufacture, in vitro diagnostic medical devices are designed, manufactured and packaged in such a way as to meet the following objectiv…
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