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Showing 1111–1120 of 31344 articles for “Art. Cass. 3e civ. 23-5-1995 n° 93-11.103”
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 health establishment authorised to carry out the activity mentioned in 3° of Article R. 6123-1 :1° Sets up the premises and equipment to allow access to vulnerable persons, in particular disabled…
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…
The authorisation holder is subject to the quality assurance obligation set out in I of Article L. 1333-19. The holder of the cross-sectional imaging authorisation must ensure that data from professio…
The holder ensures the continuity and safety of care as provided for in Article L. 1110-1, and formalises this in the protocols referred to in Article D. 6124-237.
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.
The authorisation holder must ensure that the equipment is connected to a system for archiving, sharing and distributing examinations, including images, in order to improve the quality of radiological…
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