Article R134-10
In the event of the death of a commercial agent, the obligation to apply for deregistration falls to his heirs or universal successors, through the intermediary of the single body mentioned in article…
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Showing 5231–5240 of 30748 articles for “Art. R 315-40”
In the event of the death of a commercial agent, the obligation to apply for deregistration falls to his heirs or universal successors, through the intermediary of the single body mentioned in article…
A basement may be made available for residential purposes if its characteristics do not constitute a health risk for the occupant and if it meets the following cumulative conditions:-it meets the requ…
I.-The justification for decisions to take action to prevent or reduce risks and protect people is examined when the plans referred to in Article L. 1333-13 and Chapter I of Title IV of Book VII of th…
The judgment adopting the plan is communicated by the registrar to the persons mentioned in 3° of Article R. 621-7 and is the subject of the advertisements provided for in Article R. 621-8.If the plan…
The court with jurisdiction to rule on a challenge to the appointment and election of the members of the special negotiating body is the court within whose jurisdiction the registered office of the Eu…
The members of the Economic, Social, Environmental, Cultural and Education Council are appointed for six years. In accordance with the procedure laid down in Article R. 7124-5, a vacancy shall be fill…
The employer shall appoint a person to act as an advisor on the prevention of risks associated with electromagnetic fields. This person may be the employee on whom the employer relies under article R.…
If it is established that the aid was obtained as a result of false declarations or if the condition of effective control of the company created or taken over ceases to be met within two years of the…
The duration of the suspension of approval may not exceed one month. Within this period, the commission, after the administrative authority defined in article R. 7124-1 has given the agency concerned…
As part of the procedure applicable to medical devices undergoing clinical investigations, the manufacturer shall draw up a declaration containing the information referred to in Articles R. 1123-37 to…
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