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Showing 671–680 of 40353 articles for “Art. 25-3 et seq.”
Where the conformity certification procedure applied by a manufacturer involves the intervention of an authorized body, the manufacturer may apply to the body of his choice within the framework of the…
…the manufacturer must submit to an approved body for verification the quality system which he has set up for the design, manufacture and testing of in vitro diagnostic medical devices and the applica…
The operator must ensure that the maintenance and quality controls required for the medical devices it operates are carried out. Maintenance is carried out either by the manufacturer or under his resp…
Train crews working for companies providing in-train catering or refuelling services may not be employed more than five days a week. Train crews working for companies providing sleeping accommodation…
The establishment participating in the network referred to in Article R. 6123-26 regularly sends all the members of this network, under the conditions laid down in the constituent agreement: 1° An ope…
The authorisation holder organises a multi-annual skills development plan for its professionals, tailored to the populations it cares for.
Part-time stays are organised in dedicated premises and with dedicated equipment. The medical and paramedical team can be pooled with staff from nearby full-time hospital units who have been trained i…
The medical and nursing project for prison health facilities is drawn up as part of the medical project for the institution to which they are attached.
The authorisation holder has the equipment needed to provide telehealth services.
To ensure that electroconvulsive therapy procedures are carried out, the authorisation holder guarantees: 1° Patient access to anaesthesia and post-intervention monitoring under the conditions defined…
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