Article D7343-78
In order to benefit from the compensation provided for in the first paragraph of Article D. 7343-75, the representatives must provide proof of their participation in the meetings of the negotiating co…
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Showing 4481–4490 of 62559 articles for “Art. L 430-7-1”
In order to benefit from the compensation provided for in the first paragraph of Article D. 7343-75, the representatives must provide proof of their participation in the meetings of the negotiating co…
The director of the establishment shall inform the regional director of companies, competition, consumption, labour and employment, within one month, of the action he intends to take on the observatio…
…ansit or crossing customs territory, it is prohibited to import or export narcotics without a special authorisation issued for each operation by the Director General of the Agence nationale de sécurit…
The production, including cultivation, manufacture, transport, import, export, possession, offering, transfer, acquisition or use and, in general, agricultural, craft, commercial and industrial operat…
Decisions to register homeopathic veterinary medicinal products or to suspend or cancel these registrations are made public in an extract on the website of the Agence nationale de sécurité sanitaire d…
In the case of small immediate packaging other than ampoules containing only one dose of use and on which it is impossible to include all the information provided for in Article R. 5141-74, the inform…
The inclusion of an information leaflet for the user in the packaging of a medicinal product is compulsory, unless the information mentioned in article R. 5141-77 appears directly on the outer packagi…
In the absence of observations or in the event of an inadequate response to the complaints within the time limit mentioned in the previous article, the Director General of the Agence nationale de sécu…
For the purposes of this Title, medical devices other than active implantable medical devices are divided into four classes known as Class I, Class IIa, Class IIb and Class III. Whether a device belon…
In the event of disagreement on the application of the classification rules between the manufacturer of an in vitro diagnostic medical device and an authorised body involved in the conformity assessme…
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