Article R2322-5
The person responsible for the medical management of the establishment or, failing that, for the medical management of the section of the establishment receiving pregnant women must, before taking up…
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Showing 7431–7440 of 26067 articles for “Art. Physical delivery two-event rule”
The person responsible for the medical management of the establishment or, failing that, for the medical management of the section of the establishment receiving pregnant women must, before taking up…
The authorisations and approvals provided for in articles R. 2322-2 and R. 2322-5 may only be granted to persons of good character.
The Prefect issues a receipt for the application. He will then carry out an investigation. He must notify the interested parties of his decision within two months of receiving the request.
…mmunes of the départements of Hauts-de-Seine, Seine-Saint-Denis and Val-de-Marne are subject to the rules applicable to communes subject to the provisions of this chapter and other provisions specific…
For the application of the provisions of Part Two to the communes of French Polynesia:1° The references to the prefect and the representative of the State in the department or collectivity, as well as…
The joint conciliation commission referred to in article L. 1110-3, which has jurisdiction in the event of a complaint lodged by a person who considers that he or she has been the victim of a discrimi…
Appeals against rulings on lis pendens or related actions by courts of first instance are lodged and decided in the same way as for pleas of lack of jurisdiction. In the event of multiple appeals, the…
The First President shall rule within one month of the lodging of the application at the registry, after obtaining the opinion of the Public Prosecutor.He shall issue an order rejecting the applicatio…
The Joint Committee is made up of equal numbers of employers' and employees' representatives. These representatives are appointed respectively by the professional organisations which are representativ…
In the event of disagreement on the application of the classification rules between the manufacturer of an in vitro diagnostic medical device and an authorised body involved in the conformity assessme…
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