Article R1123-3
When the Minister for Health intends to withdraw the approval of a committee, he will inform the Director General of the Regional Health Agency, who will notify the committee chairman. The latter has…
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Showing 2451–2460 of 13796 articles for “Art. European Commission report COM”
When the Minister for Health intends to withdraw the approval of a committee, he will inform the Director General of the Regional Health Agency, who will notify the committee chairman. The latter has…
…cle 3 of Decree No. 2012-1246 of 7 November 2012 on public budgetary and accounting management, the Committees for the Protection of Individuals are subject to the budgetary, financial and accounting…
The committees for the protection of individuals comprise thirty-six members divided into two colleges, each with 18 members: 1° The first college is made up of at least: a) Eight people with qualific…
The Chairman of the Personal Data Protection Committee is the authorising officer for expenditure and revenue.
The members elect the Chairman of the Committee from among their number by an absolute majority of those present. If this majority is not achieved after two ballots, the Chairman is elected by relativ…
Each committee has its headquarters in a public establishment with whose legal representative the Director General of the Regional Health Agency and the Data Protection Committee enter into an agreeme…
…formation system for research involving the human person enables: 1° Exchanges between sponsors and committees for the protection of individuals. To this end, it receives requests for advice from spon…
For all research involving humans, the sponsor must pass on to the investigators concerned any information likely to affect the safety of individuals.
The competent authority defined in Article L. 1123-12 implements the vigilance system relating to research involving the human person. Where necessary, it shall take appropriate measures to ensure the…
The investigator notifies the sponsor without delay from the day on which he becomes aware of all serious adverse events and all adverse reactions and serious incidents occurring in the course of rese…
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