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Showing 6621–6630 of 30643 articles for “Art. R 123-238”
Any medical device placed on the market or put into service in France must bear the CE mark certifying that it meets the conditions set out in article R. 5211-17. However, CE marking is not required f…
I.-The Prefect of the département, in the light of the reports made pursuant to article R. 412-14-1 or the report referred to in article R. 412-15, may issue injunctions. If the injunctions, addressed…
I.-The risk management system referred to in Article L. 354-2 comprises the strategies, processes and information procedures needed to identify, measure, monitor, manage and report, on an ongoing basi…
As part of the tasks conferred on it by Article L. 1418-1, the Agence de la biomédecine is in particular responsible for : 1° Managing the national list of patients waiting for organ and corneal trans…
I.- Advance directives are kept in a way that makes them easily accessible to the doctor called upon to make a decision to limit or stop treatment as part of the collegiate procedure defined in articl…
The report of the classification committee to which the matter has been referred characterises the work or document and, in particular, indicates the sequences or images likely to give rise to particu…
For the application of 3° of Article…
The creditor shall proceed with the seizure by serving a document on one of the persons mentioned in articles…
The term referred to in the tenth paragraph of article L. 132-23 may not exceed the shorter of eight years or the maturity date of the guarantee. Before the maturity date mentioned in article L. 134-1…
I.-When it is granted approval under the conditions set out in I of Article L. 138-2, the collective management organisation must immediately publish the following information on its website, in a ded…
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