Article R5121-178-1
This article applies to the post-authorisation safety studies referred to in Article R. 5121-178 which are carried out either voluntarily by the holder of the marketing authorisation referred to in Ar…
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Showing 8901–8910 of 31565 articles for “Art. Cass. 2ème civ. 13-6-2019 n° 18-14.954”
This article applies to the post-authorisation safety studies referred to in Article R. 5121-178 which are carried out either voluntarily by the holder of the marketing authorisation referred to in Ar…
The regional pharmacovigilance centres carry out vigilance missions relating to health products under the conditions defined in article R. 1413-61-4.
I.-This article applies to the post-authorisation studies referred to in article R. 5121-178 which are carried out by the holder of the authorisation referred to in article L. 5121-8 in order to compl…
This sub-section applies to post-authorisation safety studies of a non-interventional nature within the meaning of Article R. 1121-2, which give rise to the collection of safety information from patie…
Subject to the adaptations provided for in this Title, the following provisions shall apply in the French Southern and Antarctic Lands to concession contracts concluded by the State or its public esta…
If the foreign court's request is granted, the Ministry of Justice shall indicate the conditions under which the investigative measure is to be carried out and, where appropriate, designate the compet…
If so requested in the letter rogatory, and provided that the investigative measure prescribes that a hearing be conducted exclusively, the Ministry of Justice may authorise its direct execution by th…
The doctor, dental surgeon, midwife, pharmacist or nurse shall immediately report any adverse reaction suspected of being due to a medicinal product or to a product mentioned in article R. 5121-150 of…
…sulting from Order no. 2019-740 of 17 July 2019 L. 341-2 and L. 341-3 Resulting from the ordonnance n° 2016-301 du 14 mars 2016 L. 341-4 Resulting from the ordonnance n° 2019-740 du 17 juillet 2019 L.…
The regional pharmacovigilance centres inform the Agence nationale de sécurité du médicament et des produits de santé on the same day of the reports of adverse reactions likely to be due to a blood-de…
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