Article L773-6
…In the wording resulting from L. 511-51 Ordinance no. 2020-1635 of 21 December 2020 L. 511-52 Order 2014-948 of 20 August 2014 L. 511-53 Order no. 2014-158 of 20 February 2014 L. 511-53-1 Order no. 20…
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Showing 2281–2290 of 30371 articles for “Art. 13 mai 2014”
…In the wording resulting from L. 511-51 Ordinance no. 2020-1635 of 21 December 2020 L. 511-52 Order 2014-948 of 20 August 2014 L. 511-53 Order no. 2014-158 of 20 February 2014 L. 511-53-1 Order no. 20…
…In the wording resulting from L. 511-51 Ordinance no. 2020-1635 of 21 December 2020 L. 511-52 Order 2014-948 of 20 August 2014 L. 511-53 Order no. 2014-158 of 20 February 2014 L. 511-53-1 Order no. 20…
…des marchés financiers is the competent authority, within the meaning of Article 67(1) of Directive 2014/65/ EU of the European Parliament and of the Council of 15 May 2014 on markets in financial ins…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé: 1° Records any adverse reaction suspected to be due to a medicinal product or to a product mentioned in…
…70 ; 3° Information transmitted by the regional pharmacovigilance centres mentioned in Article R. 1413-61-4;4° Reports sent in application of article R. 5121-175 by pharmaceutical establishments, incl…
Without prejudice to the obligations laid down in Articles R. 5121-138 to R. 5121-142, the packaging of a blood-derived medicinal product includes three detachable labels, separate from the informatio…
In the establishments referred to in Article R. 5121-187, the person administering the blood-derived medicinal product to the patient completes the dispensing and administration slip with the followin…
…drug dependence and addictovigilance assessment and information centres referred to in article R. 5132-112 and the poison control centres referred to in article L. 6141-4 to provide him with any info…
…This supply is managed in accordance with the provisions of the order provided for in article R. 5132-42. When a medicinal product is taken from the supply provided for in the previous paragraph, th…
I.-The Director General of the Agence nationale de sécurité du médicament et des produits de santé, on the basis of concerns resulting from the evaluation of data from pharmacovigilance activities, in…
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