Article R4451-48
I.-The employer shall ensure that measuring instruments or devices, contamination detection devices and operational dosimeters are in good working order. II.-The employer shall periodically check thes…
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Showing 9351–9360 of 46455 articles for “Art. I bis”
I.-The employer shall ensure that measuring instruments or devices, contamination detection devices and operational dosimeters are in good working order. II.-The employer shall periodically check thes…
The medical examination provided for in Article L. 4624-2-1 is organised for the following categories of workers:1° Workers who are benefiting or have benefited from enhanced individual monitoring of…
Renewal of the work permit referred to in I of article R. 5221-1 is applied for during the second month before it expires. The renewal application must be accompanied by documents, the list of which i…
The National Council elects from among its members the members who make up the restricted panel called upon to deliberate in the cases provided for in I of article L. 4312-7. The restricted panel also…
Each candidate completes a declaration of candidacy in which he or she indicates his or her full name, date of birth, address, qualifications, method of practice, professional qualification and, where…
All medicinal products are fitted with the tamper-evident device referred to in Article R. 5121-138-2. However, this device is not compulsory for medicinal products on the list set out in Annex I to C…
The rights acquired in hours underarticle 22 quater of law no. 83-634 of 13 July 1983 may be converted into euros, at the initiative of any person mentioned in articles L. 6323-2 and L. 6323-33, withi…
In the absence of an application for authorisation submitted under the conditions of article R. 6523-2-10, or if the applications submitted do not meet the conditions laid down in I of the same articl…
A prescription for medicinal products in lists I and II may not be made for a treatment period of more than twelve months.However, for public health reasons, in the case of certain medicinal products,…
The authorisation holder is subject to the obligation of quality assurance defined in I of Article L. 1333-19. The authorisation holder shall ensure that the equipment used to expose patients to ionis…
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