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Showing 8261–8270 of 39773 articles for “Art. R. 145-5”
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…
The provisions of this section apply without prejudice to the provisions of articles R. 1221-22 to R. 1221-52 relating to haemovigilance.
…dless of the dose administered. This definition does not apply to the products mentioned in article R. 1211-29 and to labile blood products; 8° For research involving a medicinal product, unexpected a…
…of the trade union organisations whose candidacy is published pursuant to the provisions of article R. 2122-38 on the website of the Ministry of Labour with the conditions of presentation provided for…
A National Commission for Voting Operations is set up under the Minister for Labour.
…el and of the other candidate trade union organisations mentioned in the third paragraph of article R. 2122-33.
…ter for the Economy for a period of five years. This order appoints an alternate for each full member. The members mentioned in 2° to 7° are appointed on the recommendation of the Minister concerned,…
A committee responsible for issuing an opinion on the applications for authorisation referred to in article L. 313-21-1 is placed under the authority of the Minister for the Economy.
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