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Showing 241–250 of 20800 articles for “Art. D 815-6”
The authorisation decision and the decision authorising its renewal mention: 1° The name of the Maison Sport-Santé; 2° The name and legal form of the legal entity holding the authorisation; 3° The nam…
In the interests of public health, the Medical Risks Observatory analyses the data defined in the first paragraph of article L. 1142-29 for the purposes of understanding medical risks, as part of its…
The Medical Risks Observatory adopts its own rules of procedure, which set out the conditions under which it operates.
The Medical Risks Observatory may only deliberate if at least half of its members in office, including the Chairman or, in his absence, the Vice-Chairman, are present. Decisions are taken by a majorit…
The authorisation to import labile blood products for direct therapeutic use is issued by the Agence nationale de sécurité du médicament et des produits de santé to the Armed Forces Blood Transfusion…
The importation of a labile blood product or a plasma paste may be authorised only if the samples of blood or its components from which this product has been prepared meet the requirements of section…
The importer is required to: 1° Ensure that the establishment that collected or took the sample undertakes to pass on any information that could call into question the quality and safety of the produc…
…rticle L. 441-14, companies shall present in the management report : 1° For suppliers, the number and total amount of invoices received but not paid by the end of the financial year for which the due…
The chairman of the Trade Practices Review Commission may appoint one or more rapporteurs on the basis of their expertise. The commission's secretariat is provided by the Directorate-General for Compe…
The regional prefect has a period of three months in which to grant or refuse approval. The starting point for this period is set at the date of issue of the acknowledgement of receipt specifying the…
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