Article R7343-102
The Director General of the Autorité des relations sociales des plateformes d'emploi shall rule on the request for expert appraisal in the light of the application file provided for in Article R. 7343…
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Showing 7161–7170 of 38200 articles for “Art. R 210-6”
The Director General of the Autorité des relations sociales des plateformes d'emploi shall rule on the request for expert appraisal in the light of the application file provided for in Article R. 7343…
The purpose of the expert appraisal, to which one or more workers' organisations recognised as representative or one or more professional organisations of platforms recognised as representative may ha…
The Director General of the Employment Platforms Labour Relations Authority shall refer the matter to the workers' organisations recognised as representative and the professional organisations of plat…
The Director General of the Employment Platforms Labour Relations Authority shall notify the organisations that submitted the request and the expert of his reasoned decision. He shall also inform the…
The platforms' professional organisations shall provide the expert body with the information necessary for it to carry out its task within the time limits defined for each appraisal by the Director Ge…
The expert will submit his conclusions to the Employment Platforms Labour Relations Authority, which will then forward them to all the organisations representing the sector.
Once it has been established that the assignment provided for in Article R. 7343-109 has actually been carried out, the expert will be entitled to payment on the basis of the amount and payment schedu…
The manufacturer who intends to have clinical investigations carried out in France to verify the performance of a medical device or to detect any undesirable side effects, or his authorised representa…
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…
As part of the procedure applicable to in vitro diagnostic medical devices undergoing an assessment of their performance, the manufacturer must draw up a declaration containing the data enabling the d…
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