Article R5141-75
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…
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Showing 7521–7530 of 18871 articles for “Art. CA Douai 12-7-2018 n° 18/00485”
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…
…Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail. In the case of vaccines, mention of other vaccines may be authorised where this is necessary to describe th…
…administration; 4° The batch number; 5° The expiry date; 6° The words "for veterinary use". In this case, the outer packaging must include all the information specified in Article R. 5141-73.
…the company by any means that enables the date of receipt to be determined. The decision shall indicate the deadline and terms for payment of the sums in question. This notification shall include the…
In each region, a commission is responsible for issuing an opinion on animal health programmes and proposing the approval of the groups designated in the first paragraph of article L. 5143-6.
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…
The regional material vigilance and reactovigilance coordinators carry out their vigilance duties under the conditions defined in article R. 1413-61-4.
Prescriptions for medical devices issued at the request of a patient with a view to obtaining a supply in another Member State of the European Union must include the following information: 1° The surn…
…n of the country information, to 3° of Article R. 5211-70, persons legally authorised to supply medical devices may refuse to supply these products, prescribed in another Member State of the European…
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