Article D1114-42
I. - For associations approved at national level, a financial agreement is concluded under the conditions set out in II of article D. 221-35 of the Social Security Code.II. - For associations approved…
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Showing 4601–4610 of 24245 articles for “Art. 1843-4”
I. - For associations approved at national level, a financial agreement is concluded under the conditions set out in II of article D. 221-35 of the Social Security Code.II. - For associations approved…
The sponsor shall inform the National Commission for Research Involving the Human Person and the National Agency for the Safety of Medicines and Health Products without delay of situations in which it…
The depositary shall give the depositor a receipt containing the inventory of the items deposited and, where applicable, kept by the depositor in accordance with article R. 1113-3.The receipt or a cop…
Insurance contracts for the research referred to in 1° and 2° of Article L. 1121-1 guaranteeing, under the conditions provided for in Article L. 1121-10, the pecuniary consequences of the civil liabil…
The training allowance may only be paid once to the same user representative required to undergo basic training, regardless of the number of mandates held by the latter.
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 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…
For research involving medicinal products, the Director General of the Agence nationale de sécurité du médicament et des produits de santé ensures that all suspected serious unexpected adverse reactio…
The sponsor of a clinical trial, whose application has been submitted under the conditions provided for in 1 of Article 98 of the above-mentioned Regulation of 16 April 2014, may inform the designated…
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