Article R814-58-2
The third parties receiving or issuing procedural documents, referred to in the second paragraph of Article L. 814-13, expressly consent or request to use electronic communication by registering on th…
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Showing 4651–4660 of 64636 articles for “Art. CE 12-5-2022 n° 416727 and CE 27-3-2020 n° 428234”
The third parties receiving or issuing procedural documents, referred to in the second paragraph of Article L. 814-13, expressly consent or request to use electronic communication by registering on th…
The persons referred to in 2° and 3° of article R. 814-58-6 as well as their authorised employees or the persons to whom authority has been given to carry out the dematerialised procedural acts in que…
…o the provisions of this sub-section, the provisions of Title XXI of Book I of the Code of Civil Procedure apply to the electronic communication of procedural documents made possible by the electronic…
…ns shall contain, on pain of nullity, in addition to the particulars prescribed for bailiff's writs and those set out in Article 54 :
If there is a change in the designation of the accounting officer or in the terms of settlement of the contract, the purchaser shall annotate the single copy or the certificate of transferability with…
For all research involving humans, the sponsor must pass on to the investigators concerned any information likely to affect the safety of individuals.
The sponsor shall keep detailed records of all adverse events notified to it by the investigator(s). These records shall be transmitted to the competent authority mentioned in Article L. 1123-12, at i…
For the research mentioned in 1° of Article L. 1121-1 involving the cell therapy preparations defined in Article L. 1243-1, the sponsor shall report to the Agence nationale de sécurité du médicament e…
The sponsor shall inform the competent authority and the Committee for the Protection of Individuals without delay of the new facts defined in 12° of Article R. 1123-46 and, where appropriate, of the…
For the research referred to in 1° of Article L. 1121-1 concerning medical devices and in vitro diagnostic medical devices, the sponsor must report to the Agence nationale de sécurité du médicament et…
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