Article R4341-20
When the qualification or, where applicable, the authorisation to practise is registered with the regional health agency, the person concerned is issued with a professional card, the model for which i…
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Showing 1151–1160 of 65577 articles for “Art. s. L 227-1 to L 227-20”
When the qualification or, where applicable, the authorisation to practise is registered with the regional health agency, the person concerned is issued with a professional card, the model for which i…
The optician carries out all the measurements required for the manufacture of optical equipment. These measurements can be taken remotely.
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.
France Compétences is subject to the economic and financial control of the State under the conditions set out in decree no. 55-733 of 26 May 1955 relating to the economic and financial control of the…
Private training providers are not required to appoint a statutory auditor if they do not exceed the figures set for two of the three criteria defined in article R. 6352-19 for two successive financia…
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…
If the Public Prosecutor considers, following the inspector's report or the laboratory's report, and if necessary after a preliminary investigation, that proceedings should be instituted or an investi…
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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