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Showing 611–620 of 36831 articles for “Art. L 228-39”
The provisions of this sub-section may, on public health grounds, be applied, in whole or in part, to medicinal products containing substances or preparations which, although not classified as narcoti…
The marketing authorisation is renewable on application by the holder to the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail no later…
For each establishment belonging to companies mentioned in 4° to 10° of Article R. 5142-1, the number of assistant pharmacists or veterinarians is set as follows, depending on the number of staff calc…
As part of the EC declaration of conformity procedure, the manufacturer shall draw up technical documentation making it possible to assess the conformity of the medical device with the essential requi…
Each user department of a medical device on the list provided for in Article R. 5212-36 completes the information mentioned in Article R. 5212-38 by recording:-the date of use ;the identification of t…
The replacement of authorised heavy equipment mentioned in 4° or 5° of article R. 6122-26 before the authorisation expires is subject to the modification of the initial authorisation. If the nature an…
The duties of a member of the Board of Directors are performed free of charge. They are entitled to travel and subsistence allowances under the conditions set out in article R. 1413-7.
Establishments providing care for pregnant women and newborn babies include, on the same site, either an obstetrics unit, or an obstetrics unit and a neonatology unit, or an obstetrics unit, a neonato…
The formalities set out in articles R. 320-1 to R. 320-5 are deemed to have been completed once the obligations set out in articles 11 to 15-1 of the Maritime Labour Code have been met.
The birthing unit has at least one pre-delivery room equipped to receive the woman in labour, prepare her for delivery and monitor the onset of labour. The pre-labour room has the same equipment as a…
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