Article D5132-43-9
When an employer plans to conclude employment contracts that derogate, for all of its eligible employees, from the minimum weekly working time of twenty hours, it must provide the Prefect with: 1° A d…
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Showing 8591–8600 of 31530 articles for “Art. Cass. 3e civ. 19-5-1981 n° 79-14.882”
When an employer plans to conclude employment contracts that derogate, for all of its eligible employees, from the minimum weekly working time of twenty hours, it must provide the Prefect with: 1° A d…
In addition to its chairman, the Disciplinary Chamber of First Instance comprises:1° Two full members and two alternate members elected by the regional or inter-regional council from among its members…
The provisions of article R. 4124-5 are applicable to elections to the disciplinary chambers of first instance for chiropodists.
When the services responsible for monitoring the performance of the contract or the monitoring agents referred to in Article L. 6361-5 find that the employer has failed to comply with the provisions o…
The employer is notified of the decision to withdraw the benefit of the exemption. The employer informs the staff representatives. It is also sent to the body responsible for collecting social securit…
In order to comply with the essential requirements relating to design and manufacture, active implantable medical devices must be designed, manufactured and packaged in such a way as to meet the follo…
In order to comply with the essential requirements relating to design and manufacture, medical devices, other than active implantable devices, must be designed, manufactured and packaged in such a way…
Before applying for the issue of the EC design examination certificate or EC type examination certificate referred to in Articles R. 5211-40 and R. 5211-41 respectively, manufacturers of medical devic…
The manufacturer is required to update the risk analysis and management system referred to in Article R. 5211-23-2 by analysing all elements relating to the medical devices he manufactures and taking…
Medical devices must be designed and manufactured, taking into account the generally recognised state of the art, in such a way that, when used in accordance with their intended purpose and under the…
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