Article R6144-5-1
The duties of the chairman of the hospital medical board end when he resigns and submits his resignation to the chairman of the hospital board or when the term of office of the hospital medical board…
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Showing 3501–3510 of 33529 articles for “Art. Cass. com. 18-5-2017 n° 15-28.683”
The duties of the chairman of the hospital medical board end when he resigns and submits his resignation to the chairman of the hospital board or when the term of office of the hospital medical board…
In addition to the Director, who chairs it, the person in charge of human resources management and staff representatives, the Management Committee includes a representative of the region appointed by…
Each centre shall have an administrative social committee and, where applicable, a specialised health, safety and working conditions committee, reporting to its Director, under the conditions laid dow…
Notwithstanding article 6 of the above-mentioned decree of 20 November 2020, the social committee of each centre is created by a decision of its board of directors.
If there is a change in the designation of the accounting officer or in the terms of settlement of the contract, the purchaser shall annotate the single copy or the certificate of transferability with…
For all research involving humans, the sponsor must pass on to the investigators concerned any information likely to affect the safety of individuals.
The sponsor shall keep detailed records of all adverse events notified to it by the investigator(s). These records shall be transmitted to the competent authority mentioned in Article L. 1123-12, at i…
For the research mentioned in 1° of Article L. 1121-1 involving the cell therapy preparations defined in Article L. 1243-1, the sponsor shall report to the Agence nationale de sécurité du médicament e…
The sponsor shall inform the competent authority and the Committee for the Protection of Individuals without delay of the new facts defined in 12° of Article R. 1123-46 and, where appropriate, of the…
For the research referred to in 1° of Article L. 1121-1 concerning medical devices and in vitro diagnostic medical devices, the sponsor must report to the Agence nationale de sécurité du médicament et…
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