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Showing 881–890 of 25706 articles for “Art. Cass. com. 17 December 1991 · Cass. com. 12 November 1992 · Cass. 3e civ. 24 November 1987”
As part of the EC declaration of conformity procedure, the manufacturer shall draw up technical documentation making it possible to assess the conformity of the in vitro diagnostic medical device with…
A form, the model for which is approved by the Minister for Health, is drawn up by the emergency department and sent to the director of the establishment to report any malfunction observed in the orga…
…ce of complaints alleging an infringement or failure to comply with the provisions of Articles L. 8112-1 and L. 8112-2, except where the complainant has informed his employer in writing that he is see…
Drivers are entitled to periodic single rest periods of at least thirty-five hours, or double rest periods of at least fifty-nine hours. The number of rest days per twenty-eight day period is set by c…
The authorisation holder is subject to the obligation of quality assurance defined in I of Article L. 1333-19.
The performance of any complex medical procedure must comply with recommendations for good practice or be the subject of a collegiate decision.
…The holder of the authorisation for activities covered by category C as provided for in article R. 6123-166 must ensure that the paramedical team is trained in cancer care. II - The provisions of arti…
The general organisation, equipment and premises of the authorisation holder are appropriate to the nature and volume of the services provided.
…lder of an authorisation for activities covered by category D, as provided for in 4° of Article R. 6123-166 , carries out the treatments mentioned in Article R. 6123-32-1, falling within the scope of…
The authorisation holder ensures that data from professional practices is collected and analysed with the aim of improving practices and risk management.
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