Article L1111-22
The collection, exchange or sharing of personal health data necessary for the management of a patient in the course of care provided while the patient is present on the territory of another Member Sta…
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Showing 9201–9210 of 45512 articles for “Art. Rép. Rabault: AN 25-2-2020 n° 24560”
The collection, exchange or sharing of personal health data necessary for the management of a patient in the course of care provided while the patient is present on the territory of another Member Sta…
…nt of shared health information systems is funded by a contribution from the compulsory health insurance schemes. The amount of this contribution is set by order of the Minister for Social Security. T…
When public prosecution has been initiated by the public prosecutor or the injured party, and subject to the victim's agreement, associations approved at national level under the conditions set out in…
…l d'Etat, issued after consultation with the Commission nationale de l'informatique et des libertés and the national councils of the health professions, shall set the conditions for application of the…
The provisions of Section 3 of Chapter III of Title II of Law No. 78-17 of 6 January 1978, as amended, relating to information technology, files and freedoms, as well as the provisions of Regulation (…
…d out at the Institution nationale des invalides or in a health establishment or army hospital with an in-house pharmacy, failure by the sponsor to communicate in advance to the pharmacist managing th…
I.- Unemancipated minors, protected adults or adults who are unable to express their consent and who are not the subject of a legal protection measure shall, when their participation in research invol…
In the context of a clinical investigation involving an intervention that is not justified by the patient's usual care and that involves risks and constraints that are not minimal, failure by the spon…
The competent authority may, at any time, request additional information on the clinical investigation from the sponsor. Where the competent authority considers that the requirements set out in Regula…
No research involving the human person may be carried out :- if it is not based on the latest scientific knowledge and on sufficient pre-clinical experimentation ;- if the foreseeable risk incurred by…
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