Article R5425-20
Tasks of general interest are deemed to be those which, on the proposal of a public authority or a private not-for-profit organisation, have been approved by the prefect of the département in which th…
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Showing 1421–1430 of 65597 articles for “Art. L 141-7 · Cass. com. 20 June 1978 · CA Versailles 17 December 1980 · Cass. com. 14 May 1952 · Cass. 1re civ. 2 March 1960 · C. civ. Art. 2276”
Tasks of general interest are deemed to be those which, on the proposal of a public authority or a private not-for-profit organisation, have been approved by the prefect of the département in which th…
The optician carries out all the measurements required for the manufacture of optical equipment. These measurements can be taken remotely.
The detailed rules for the application of sections 1 to 12 of this chapter are determined as necessary, after obtaining the opinion of the Director General of the Agence nationale de sécurité du médic…
Blood establishments and organisations or companies manufacturing or exploiting blood-derived medicinal products which are aware of information likely to cast doubt on the quality of blood or plasma i…
Without prejudice to the provisions of Chapter III of Title III of Book V of the Environment Code, the provisions of Articles R. 1243-34 to R. 1243-38 are applicable to the conditions for authorisatio…
For the purposes of this sub-section, army hospitals and the army blood transfusion centre are regarded as public health establishments and blood transfusion establishments respectively.
A regulation, drawn up with the agreement of the regional prefect by each mission responsible for the pedagogical supervision of apprenticeship training leading to a diploma and the relevant chamber o…
…atutory auditor if they do not exceed the figures set for two of the three criteria defined in article R. 6352-19 for two successive financial years.
Any operation relating to the processing mentioned in article R. 6351-13 is recorded, including the identification of the user, the date and the nature of the intervention in this processing. These re…
The labelling of a medical device given to the end user or patient, the accompanying leaflet and any other information relating to its operation or use must include a version written in French.
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