Article R1333-127
The authorisation to manufacture or use a high activity sealed source sets out in particular:1° Requirements relating to the organisation of radiation protection and the allocation of responsibilities…
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Showing 1451–1460 of 5857 articles for “Art. 12 juill. 2018”
The authorisation to manufacture or use a high activity sealed source sets out in particular:1° Requirements relating to the organisation of radiation protection and the allocation of responsibilities…
I.-If the application relates to the use of ionising radiation for medical purposes, the supporting documents to be included in the authorisation application file are supplemented by the information m…
…armaceuticals with a view to their distribution, generators or precursors as defined in Article L. 5121-1, the application for authorisation shall be accompanied by a document establishing that an app…
The French Nuclear Safety Authority (Autorité de sûreté nucléaire) gives its decision on applications for authorisation within six months. This period may be extended twice for the same duration by th…
The provisions of this subsection apply to nuclear activities subject to registration pursuant to Article R. 1333-113 or to authorisation pursuant to Article R. 1333-118.
In the cases provided for in 1° of VI of Article L. 1333-9, information on the means and measures taken to protect against malicious acts is not provided as part of the application for authorisation.
Anatomical parts of animal origin intended for abandonment are sent to rendering plants in accordance with the provisions of the French Rural and Maritime Fishing Code.
A copy of the lead exposure risk report must be provided by the owner or operator of the accommodation in order to inform the occupants and persons required to carry out work, as required by article L…
For its application in Saint-Barthélemy, the first paragraph of article R. 1336-2 reads as follows: "Checks on the application of the provisions of article R. 1336-1 and the decree adopted for their a…
Health professionals and manufacturers, importers, downstream users and distributors of substances or mixtures are required to provide, at the request of the bodies responsible for toxicovigilance, re…
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