Article D6325-19-1
The exemption provided for in Article L. 6325-17 applies to groups of employers for integration and qualification receiving the aid provided for in Articles D. 6325-23 and D. 6325-24.
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Showing 7131–7140 of 17962 articles for “Art. 5 avr. 2011”
The exemption provided for in Article L. 6325-17 applies to groups of employers for integration and qualification receiving the aid provided for in Articles D. 6325-23 and D. 6325-24.
…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 of Article L. 1111-3, relating to…
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…
…paid hours taken into account for the calculation of the exemptions provided for in articles L. 6325-16 and L. 6325-17 is equal to the product of the working hours that the employee would have worked…
…erties making it possible to guarantee the characteristics and performances mentioned in Article R. 5211-21, in particular as regards the reliability of the device control systems and the compatibilit…
…erties which enable them to guarantee the characteristics and performance referred to in Article R. 5211-21, to reduce as far as possible the risks presented by contaminants and residues for patients,…
…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 devices or active implantable medical…
…anufacturer 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 accou…
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…
…gust 2012 on specific requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC for active implantable medical devices and medical devices manufactured utilisin…
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