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Showing 2111–2120 of 51623 articles for “Art. I.5°”
The manufacturer is required to update the risk analysis and management system referred to in Article R. 5211-23-2 by analysing all elements relating to the medical devices he manufactures and taking…
Medical devices must be designed and manufactured, taking into account the generally recognised state of the art, in such a way that, when used in accordance with their intended purpose and under the…
Medical devices and active implantable medical devices manufactured from non-viable tissues of animal origin or non-viable products derived from tissues of animal origin, falling within the scope defi…
The conditions for implementing the essential requirements defined in this section are specified, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produ…
The ordinary remedies are appeal and opposition, the extraordinary remedies are third-party opposition, application for review and appeal in cassation..
In the event of a dispute relating to the application of the provisions of articles L. 111-1, L. 111-2, L. 111-4 and L. 111-4-1, it is up to the professional to prove that he has fulfilled his obligat…
As soon as the connection is established, pits and other similar installations must be put out of use or prevented from creating future nuisances, by the owner and at his expense.
Pursuant to the provisions applicable in the Moselle, Bas-Rhin and Haut-Rhin départements, the following also constitute enforceable titles: 1° Deeds drawn up by a notary in these three départements w…
The movable and immovable property allocated to the public mental health services and required to carry out their activities is made available to the establishments mentioned in article L. 3221-4 desi…
The Minister of Defence is competent to recognise a qualification different from the one initially recognised for practitioners in the armed forces covered by the provisions of article L. 4138-2 of th…
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