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Showing 9061–9070 of 17894 articles for “Art. 5 nov. 2003”
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…
Once a year for the duration of the research referred to in 1° of Article L. 1121-1 or on request, the sponsor must send the competent authority defined in Article L. 1123-12 and the relevant Data Pro…
The form, content and procedures for reporting adverse reactions and new facts as defined in Article L. 1123-10 and, where applicable, the procedures for lifting the blind shall be laid down by decisi…
…visions of this section apply without prejudice to the provisions of articles R. 1221-22 to R. 1221-52 relating to haemovigilance.
…of an in vitro diagnostic medical device and harmful to the health of a person undergoing research; 5° Adverse effect of a cosmetic product or a tattoo product, any harmful and undesired reaction occu…
…of Labour with the conditions of presentation provided for in the last paragraph of article R. 2122-52, when these propaganda documents are common to more than one region; 2° Ensuring that electors ar…
A National Commission for Voting Operations is set up under the Minister for Labour.
The National Commission for Voting Operations comprises :1° Two civil servants appointed by the Minister for Labour, one of whom acts as chairman and the other as secretary ;2° The representatives of…
…r Small and Medium-sized Enterprises;4° A representative of the Minister for the Solidarity Economy;5° A representative of the Minister for Industry;6° A representative of the Minister responsible for…
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