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Showing 1851–1860 of 38431 articles for “Art. L 221-15”
The time limits set by articles R. 7343-12 and R. 7343-14 are calculated and extended in accordance with the provisions of articles 640 to 642 of the Code of Civil Procedure.
The decision to withdraw authorisation is published in the prefecture's registry of administrative acts. The prefect will inform the president of the departmental councils concerned, the minister resp…
The national monitoring, support and control group carries out or provides support for operations requiring special expertise, assistance for departments, specific control or coordination of controls.…
On receipt of the sample(s), as appropriate, the Agence nationale de sécurité du médicament et des produits de santé or the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement…
The provisions of articles R. 5122-5, R. 5122-6, R. 5122-7, R. 5122-9 and R. 5122-13 to R. 5122-16 are applicable to condom advertising. Applications for approval must be accompanied either by the cer…
For the purposes of this chapter, "establishment" means any place or site where one or more operations involving micro-organisms and toxins or products containing them are carried out.
The application for marketing authorisation is accompanied by a draft summary of product characteristics, the presentation and content of which are laid down in accordance with Article 14 of Directive…
The affixing of marks or inscriptions on a medical device, on its packaging or on the instructions for use which are likely to mislead as to the meaning or form of the CE marking is prohibited. Any ot…
The provisions of article R. 5211-21 are applicable to in vitro diagnostic medical devices.
Local reactovigilance correspondents are responsible for : 1° Recording and analysing any reported incident or risk of incident likely to be due to an in vitro diagnostic medical device; 2° Declaring…
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