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Showing 1301–1310 of 37577 articles for “Art. L 232-23”
An order by the Minister for Labour sets the procedures and period for the submission of applications by candidate organisations, as well as the model documents required for the submission of applicat…
After checking the integrity of the seals, the two experts are given the sample previously held by the owner or holder and the sample previously held by the agent who took the sample and forwarded to…
The conditions under which List I and List II medicinal products are prescribed, held or distributed may, on public health grounds, be made subject, in whole or in part, to the provisions of sub-secti…
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…
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