Article R1123-71
…n referred to in Article R. 1123-20 ; 2° Where applicable, the pharmaceutical form, batch number(s) and expiry date of the medicinal product(s) required for the research;3° Where applicable, for the m…
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Showing 241–250 of 60773 articles for “Art. 1352-6 and 1352-7”
…n referred to in Article R. 1123-20 ; 2° Where applicable, the pharmaceutical form, batch number(s) and expiry date of the medicinal product(s) required for the research;3° Where applicable, for the m…
…cle L. 6331-55, within the limit of the rate mentioned in the second paragraph of the same article, and transfer it to France Compétences. II -France Compétences allocates the proceeds of this contrib…
…lves, in particular weighing, monitoring blood pressure, preparing the dialysis machine, connecting and disconnecting the extracorporeal circulation circuit and starting the automatic disinfection of…
Back-up is provided in a haemodialysis centre or in a medicalised dialysis unit under the conditions set out in article D. 6124-67. When it is provided for by agreement, this agreement mentions the nu…
…the end of the research involving the human person or its interruption, a final report is drawn up and signed by the sponsor and the investigator, and in the case of multicentre research, by all the…
…f the end of the research involving human subjects, the sponsor must inform the competent authority and the relevant data protection committee of the effective date of the end of the research, corresp…
In application of the third paragraph of article L. 1123-11, except in the case of imminent risk, the sponsor has a period of one week in which to submit its observations from receipt of the request t…
…cate this action plan to the competent authorities of the other Member States of the European Union and to the European Commission. The sponsor shall report to the competent authority and to the relev…
The competent authority shall inform without delay the Committee for the Protection of Individuals and the National Commission for Research Involving the Human Person and, for the research mentioned i…
The documents and data relating to the research are kept by the sponsor and the investigator for a period set by order of the Minister for Health issued on a proposal from the Director General of the…
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