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Showing 1191–1200 of 37567 articles for “Art. L 1221-23”
I. - For the application of 1° of article R. 5141-18 , when reference is made to published scientific literature, the experts shall justify the use of this bibliographical documentation and demonstrat…
In order to comply with the essential requirements relating to design and manufacture, active implantable medical devices must be designed, manufactured and packaged in such a way as to meet the follo…
As part of the procedure applicable to in vitro diagnostic medical devices undergoing an assessment of their performance, the manufacturer must draw up a declaration containing the data enabling the d…
Manufacturers of medical devices and the companies and organisations operating these devices shall, at the reasoned request of the Director of the Agence nationale de sécurité du médicament et des pro…
The establishment keeps a continuous chronological register in the emergency department, showing the identity of patients admitted, the day, time and method of their arrival, their referral or hospita…
This section applies to the staff of companies providing catering on trains and companies operating sleeping accommodation on trains.
The authorisation holder shall put in place a formalised organisation describing, depending on the situation, the procedures for the intervention of one or more doctors specialising in anaesthesia and…
Protocols are drawn up by the medical staff mentioned in I of article D. 6124-235 to organise patient care with the doctors in charge of the inpatient units, the continuous monitoring unit, the intens…
In order to carry out activities falling under categories B, C and D as defined in Article R. 6123-166, the holder of the authorisation for interventional radiology must have at least one intervention…
The holder of the authorisation has at least one emergency trolley on the premises for the treatment of patients requiring it.
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