Article R8122-4
The departmental directorates for employment, labour and solidarity, the departmental directorates for employment, labour, solidarity and population protection and the departmental units of the Ile-de…
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Showing 6971–6980 of 62890 articles for “Art. 386-1 to 386-4”
The departmental directorates for employment, labour and solidarity, the departmental directorates for employment, labour, solidarity and population protection and the departmental units of the Ile-de…
The Labour Inspectorate official's formal notices and requests for verification are notified to the employer in writing, either by hand-delivery against receipt, or by registered letter with acknowled…
…three samples, one left with the owner or holder of the product, the second destined for the laboratory competent to carry out the analyses and the third retained by the agent who took the sample.
The Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail may also suspend, for a period not exceeding one year, or revoke a marketing auth…
Decisions to grant, automatically vary, refuse, renew or revoke marketing authorisations subject to the national procedure are taken in accordance with the procedures laid down in Article R. 5141-27 r…
The decision to suspend, revoke or vary the marketing authorisation must state the reasons on which it is based and indicate the appeal procedures and deadlines. Except in cases of urgency, the decisi…
Independently of decisions to suspend, modify or withdraw authorisations and as a precautionary measure, the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'envi…
…EC declaration of conformity procedure, production quality assurance, the manufacturer shall submit to an authorised body for verification the quality system which he has set up for the manufacture of…
…s or medical devices in Class III or Class II b, the manufacturer shall take all necessary measures to ensure that the manufacturing process guarantees conformity of the medical devices manufactured w…
…dical devices or medical devices in class IIb or class III, the manufacturer submits an application to the authorised body for assessment of this quality system, which includes technical documentation…
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