Article R6147-58
The provisions of chapter II of title I of this book and those of chapters I to VI of this title are applicable to the Centre hospitalier national d'ophtalmologie des Quinze-Vingts subject to the prov…
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Showing 2981–2990 of 51623 articles for “Art. I.5°”
The provisions of chapter II of title I of this book and those of chapters I to VI of this title are applicable to the Centre hospitalier national d'ophtalmologie des Quinze-Vingts subject to the prov…
When providing systemic cancer treatment by immunotherapy or innovative therapeutic medicinal products, the holder of the authorisation for systemic cancer treatment has a patient care organisation wh…
I-Treatment of cancer by systemic medicinal treatments for cancer consists, within the authorised site : 1° The development of a therapeutic proposal in a multidisciplinary consultation meeting, follo…
I. - Establishments authorised for systemic medicinal treatments for cancer with designation B or C must have on site : 1° The organisation of a medical permanence at least by means of operational on-…
The establishment authorised to provide systemic medicinal treatments for cancer with a C rating complies with the obligations imposed on holders of authorisations for medicine caring for children and…
I. - When it has adopted a resolution measure in respect of a person referred to in I of Article L. 613-34, the resolution board shall fulfil the obligations set out in II and III as soon as circumsta…
I.-The agglomeration community automatically exercises the following competencies in place of the member municipalities: 1° In terms of economic development: economic development actions under the con…
I. - The application for an import authorisation for therapeutic purposes, provided for in the first paragraph of II of Article L. 1245-5, is sent by the legal entities or natural persons mentioned in…
Judicial authorities, as well as authorised judicial police officers, seized in the context of proceedings mentioned in 2° of Article 706-25-9 or notified in accordance with article R. 50-54, as well…
I.-The criteria for classifying a situation as a risk in the management of a patient's state of health due to the unavailability of a medical device shall be laid down by regulation.The manufacturers…
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