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Showing 311–320 of 37768 articles for “Art. Loi 89-462 du 6-7-1989”
Authorised bodies shall inform the Director General of the Agence nationale de sécurité du médicament et des produits de santé of all certificates issued, modified, supplemented, suspended, withdrawn…
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…
The decisions taken by the approved bodies under the procedures referred to in subsections 5, 6, 8 and 9 of section 6 of this chapter are valid for five years. They may be renewed for five-year period…
Where the authorised body encounters difficulties in implementing the conformity assessment procedures, it shall refer the matter to the Director General of the Agence nationale de sécurité du médicam…
…on of the mandataire à titre posthume, definitively determined within six months of the death, is deductible from the assets of the estate up to a limit of 0.5% of the managed estate assets. This dedu…
Notwithstanding the provisions of 1° of article R. 6152-35, practitioners carrying out their duties in a public health establishment located in an overseas department, Saint-Barthélemy, Saint-Martin,…
The competent authority in the cases provided for in article R.* 632-2 is the State representative.
As an exception to the provisions of Title I of Book II, in particular articles 240 and 248, first paragraph, and subject to the provisions of Article 698-7, the assize court provided for by articles…
…hospital medical committee ensures that the committee operates smoothly. In order to carry out its duties, the Institutional Medical Committee shall draw up its own rules of procedure in accordance w…
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