Article R4451-125
…ody accredited by the French Accreditation Committee or by any other body mentioned in Article R. 4724-1; 2° For the body competent in radiation protection, a certification issued by a certifying body…
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Showing 3311–3320 of 23443 articles for “Art. Cass. 1re civ. 13 April 1999 · Cass. 1re civ. 13 July 2004 · Cass. 3e civ. 24 June 1971”
…ody accredited by the French Accreditation Committee or by any other body mentioned in Article R. 4724-1; 2° For the body competent in radiation protection, a certification issued by a certifying body…
When, in the light of the results of individual dosimetric monitoring, the exposure of a worker has exceeded one of the dose limit values set in Article R. 4451-6, the Institut de Radioprotection et d…
…or each medicinal product or each product for which the marketing authorisation was issued after 21 July 2012; 2° Monitors the results of the risk reduction measures described in the risk management p…
For the medicinal products mentioned in 1° of II of article L. 5121-12 and in II of article L. 5121-12-1, the obligations set out in article R. 5121-161 and articles R. 5121-166 to R. 5121-170 are car…
Any company or organisation exploiting a medicinal product or a product mentioned in Article R. 5121-150 shall implement a pharmacovigilance system in order to fulfil its pharmacovigilance obligations…
…substances by the European Medicines Agency in application of Article 27 of Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004.
…he drug dependence and addictovigilance assessment and information centres mentioned in Article R. 5132-112 are responded to fully and promptly;7° Provide the Director General of the Agence nationale…
The holder of the authorisation provided for in Article L. 4211-6 is required to report the following to the Director General of the Agence nationale de sécurité du médicament et des produits de santé…
…product or a product mentioned in Article R. 5121-150 which informs, in application of Article L. 5124-6, the Director General of the Agence nationale de sécurité du médicament et des produits de sant…
By way of derogation from the provisions of Article R. 5121-168, any company or organisation exploiting an authorised or registered medicinal product or product, in accordance with the procedure laid…
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