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Showing 1891–1900 of 51426 articles for “Art. s. L 623-24 to L 623-26”
The conditions for implementing the essential requirements defined in this section are specified, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produ…
The Agence nationale de sécurité du médicament et des produits de santé submits to its control a sample of each batch of the substance which, if used separately from the medical device in which it is…
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…
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 performance of any complex medical procedure must comply with recommendations for good practice or be the subject of a collegiate decision.
I.-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 a…
The authorisation holder shall put in place a procedure to ensure that each member of the team has mastered the requirements of their duties before taking up any independent post. This procedure takes…
The general organisation, equipment and premises of the authorisation holder are appropriate to the nature and volume of the services provided.
The holder 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 sco…
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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