Article R5121-200
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…
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Showing 2211–2220 of 69041 articles for “Art. s. L 227-20-1 and L 235-9”
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…
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.
…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…
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 members of the College are subject to the provisions of Article L. 1451-1.At each meeting, the members of the College shall state, if applicable, that they have a direct or indirect family, profes…
Except for the purposes of constituting the solvency margin referred to in Article L. 385-2, supplementary occupational pension funds shall not take out loans or act as guarantors for third parties. T…
Other than the persons mentioned respectively in Article L. 631-4 and in the first and second paragraphs of Article L. 631-5 or to Article L. 640-4 and the first and second paragraphs of Article L. 64…
For an authorised establishment, the addition of a new activity within the meaning of Article R. 5124-2 is subject to an application for authorisation examined under the conditions set out in Article…
The holder of the pharmaceutical record may exercise the right of access to data concerning him or her provided for in Article 15 of Regulation (EU) 2016/679 of the European Parliament and of the Coun…
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