Article R561-22-1
For the application of Articles L. 561-7, L. 561-20, 3° of Article R. 561-5-2, 2° of Article R. 561-5-3 and Article R. 561-9, the persons mentioned in Article L. 561-2 concerned shall assess the level…
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Showing 471–480 of 67746 articles for “Art. L 581-4 and R 581-22”
For the application of Articles L. 561-7, L. 561-20, 3° of Article R. 561-5-2, 2° of Article R. 561-5-3 and Article R. 561-9, the persons mentioned in Article L. 561-2 concerned shall assess the level…
For the application of 2° of Article L. 561-10 and Article L. 561-13, in the event of a transaction involving the exchange of any means of payment, chips, tokens or tickets where the amount exceeds 2,…
A judge appointed by the first president of each court of appeal from among the judges of the court is responsible for responding to any request for an opinion on an ethical issue that the president o…
In the event of a vacancy on the committee provided for in article R. 6322-20 for a period of more than six months, the Director General of the Regional Health Agency shall appoint a mediator from amo…
Repeat offences under article R. 5232-21 are punishable in accordance with articles 132-11 and 132-15 of the French Criminal Code.
The functionalities and approval procedures for the process enabling placement under mobile electronic surveillance are determined by the dispositions de l'article R. 544-7 du code pénitentiaire.
When informed by the holder of a marketing authorisation granted under 1°, 2° or 3° of Article R. 5141-20, before the marketing of the veterinary medicinal product concerned, of the fact that for all…
Prior to any contentious proceedings, disputes relating to the decisions mentioned in article R. 6154-20 must be submitted to the Minister for Health within two months of notification.
The manufacturer, importer or any other person responsible for placing the equipment on the market shall draw up the technical file provided for in Article R. 4313-6 for each type of machine or person…
For the purposes of placing on the market in vitro diagnostic medical devices other than those subject to a performance evaluation, manufacturers shall follow the following procedures: 1° For in vitro…
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