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Showing 2971–2980 of 64883 articles for “Art. V-al. 1 to 4”
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 provisions of this section apply without prejudice to the provisions of articles R. 1221-22 to R. 1221-52 relating to haemovigilance.
For the purposes of this section, the following definitions shall apply 1° Adverse event, any noxious occurrence in a person who undergoes research involving the human person, whether or not this occu…
…f the liquidation sale by the declarant throughout its duration; the order mentioned in Article R. 310-2 sets out the terms and conditions of this display.
Any joint stock company participating in a merger operation shall make the following documents available to its shareholders at its registered office at least thirty days before the date on which the…
…ies register notifies the Conseil des maisons de vente of the striking off of a manager of the operator when this has been ordered after the updating of the criminal record has revealed the existence…
The communauté de communes is formed either without a fixed term or for a term determined by the decision instituting it.
…presence of dangerous solid or liquid products, in particular vats or tanks containing flammable or toxic liquids, it is halted until these products are removed and the installations are neutralised b…
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