Article D4122-4-2
…nseil national de l'ordre des sages-femmes respectively, is responsible for evaluating the practice of refusing care by healthcare professionals registered with each of these orders.These commissions…
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Showing 4891–4900 of 60191 articles for “Art. avis 2013-027 of 4 October 2013”
…nseil national de l'ordre des sages-femmes respectively, is responsible for evaluating the practice of refusing care by healthcare professionals registered with each of these orders.These commissions…
The committees referred to in article D. 4122-4-2 each comprise thirteen members:1° The President of the Conseil national de l'ordre or his representative ;2° Six doctors, dental surgeons or midwives…
The notice referred to in the first paragraph of article L. 143-2-2 contains the following information 1° The name, country of origin and name of the authority responsible for supervising the suppleme…
…musical works may terminate that authorisation in the event that the organisation does not grant or offer to grant such exploitation authorisations in respect of those works and has not allowed anothe…
…shall communicate, by electronic means and within a period not exceeding one month, to the holders of rights managed by the organisation in any capacity whatsoever, to organisations on whose behalf t…
A fine of €3,750 shall be imposed for delivering or selling : 1° Corrective ocular contact lenses in disregard of the conditions for delivery to a first-time wearer set out in article L. 4362-9-1 ; 2°…
…gional Director for Business, Competition, Consumer Affairs, Labour and Employment within one month of the date on which the parties concerned were notified of the decision.
…ir request, to the project manager, the labour inspectorate, agents from the prevention departments of social security organisations, agents from the Organisme Professionnel de Prévention du Bâtiment…
The logbook is kept by the coordinator for a period of five years from the date of acceptance of the work.
In the case of active implantable medical devices or medical devices in Class III or Class II b, the manufacturer shall take all necessary measures to ensure that the manufacturing process guarantees…
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