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Showing 4981–4990 of 58474 articles for “Art. 17 January 2020 · Law 89-462 of 6 July 1989”
The approved body may require the manufacturer to provide any information and to carry out any test or assessment necessary for it to carry out the verifications for which it is responsible.
Where an authorized body finds that the requirements of this Title applicable to this device have not been met or are no longer being met by the manufacturer, or where a certificate should not have be…
…mplementing the conformity assessment procedures, it shall refer the matter to the Director General of the Agence nationale de sécurité du médicament et des produits de santé for specific recommendati…
…eedings against the judgment granting the application for revision are admissible only in the event of fraud attributable to the donee or legatee. The revocation or reversal of the contested judgment…
The professional activity of hearing aid acoustician may only be carried out in premises reserved for this purpose and fitted out, in accordance with conditions laid down by decree, to enable the prac…
…he Supervisory Board, the Institutional Medical Committee and the Institutional Technical Committee of the results of the use made of these documents.These questionnaires are kept on file and may be c…
…med by the liaison letter provided for in article R. 1112-1-2 after the patient has been discharged of the medical prescriptions to which the patient must continue to adhere. He will be given any info…
Subject to the provisions of article L. 1111-5, with the exception of minors and involuntary patients, patients may, at their request, leave the establishment at any time. If the doctor in charge of t…
When a patient is at the end of their life, they are transferred home if they or their family so wish.
The hospital administration will provide hospitalised patients with a full list of land-based medical transport companies in the département.
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