Article R2272-17
The opinions issued by the sub-committees defined in article R. 2272-10 are valid if more than half or, for the sub-committees mentioned in 4° and 6° of this article, if more than one third of the mem…
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Showing 551–560 of 32624 articles for “Art. R. 232-17”
The opinions issued by the sub-committees defined in article R. 2272-10 are valid if more than half or, for the sub-committees mentioned in 4° and 6° of this article, if more than one third of the mem…
…ents, public establishments or bodies responsible for a public service mission mentioned in Article R. 1461-12 shall keep an up-to-date list and characteristics of the projects involving individual da…
…the employer or the branch shall send the competent administrative authority mentioned in article R. 5212-15: 1° The annual reports and the summary report of the actions carried out under the agreem…
…of a period of three clear days following the date on which the association referred to in article R. 512-3 is informed by the guarantor of the cessation of the guarantee. In all the cases provided f…
…al is in question shall be made in the forms and according to the procedure provided for in article R. 631-3 or R. 631-4, as applicable. The same applies when an application for the dismissal of one o…
…osis and no therapeutic alternative. By way of derogation from the first paragraph of II of article R. 1123-20-1, the Committee for the Protection of Individuals responsible for giving an opinion on t…
…titute for Radiological Protection and Nuclear Safety or by an approved body referred to in Article R. 1333-172. This authority sets the time limit within which the Institute for Radiological Protecti…
…hospital centre are each responsible for the application of the regulations provided for in article R. 6142-16. However, in order to ensure the safety of patients and all the facilities of the hospita…
…if the request is not made by the applicant or the proprietor of the patent, by the consent of either. The provisions of Article R. 612-10 are applicable. If an erroneous designation of the inventor h…
…s to post-authorisation safety studies of a non-interventional nature within the meaning of Article R. 1121-2, which give rise to the collection of safety information from patients or healthcare profe…
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