Article R1111-51
…al health space and who is at the origin of the recording of the data in the shared medical record; 3° With the Caisse nationale de l'assurance maladie under the conditions defined by the latter, in c…
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Showing 2131–2140 of 60229 articles for “Art. 35 I-5° bis · CAA Paris 3 October 2019”
…al health space and who is at the origin of the recording of the data in the shared medical record; 3° With the Caisse nationale de l'assurance maladie under the conditions defined by the latter, in c…
Without prejudice to the provisions of article R. 1111-33, when the holder is a minor, he/she may ask the healthcare professional or institution which supplies his/her shared medical record that the d…
The national contact point for e-health in France is designated by the Minister for Health. It deals with requests for access to the health data mentioned in article R. 1111-55 from a national contact…
…come from property assets, including rental income from furnished property, as referred to in 1° to 3° and 5° of I of Article L. 214-36 in the case of a société de placement à prépondérance immobilièr…
…waiver on a case-by-case basis, the amount of cash receivable from assets referred to in 1°, 2°, 2° bis and 2° ter of A of Article R. 332-2 which are subject to early investment transactions in securi…
For all research involving humans, the sponsor must pass on to the investigators concerned any information likely to affect the safety of individuals.
…igator(s). These records shall be transmitted to the competent authority mentioned in Article L. 1123-12, at its request.
…ntioned 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 et des produits de s…
…ee for the Protection of Individuals without delay of the new facts defined in 12° of Article R. 1123-46 and, where appropriate, of the measures taken. The sponsor shall inform the Director General of…
…the action of implementing the medical device, as well as the new facts mentioned in Article L. 1123-10, the relevant additional information is sent to the Agence nationale de sécurité du médicament…
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