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Showing 6261–6270 of 33647 articles for “Art. 1231 to 1231-7”
The authorisation referred to in article D. 1221-58 indicates in particular the name and address of the supplier establishment, the natural or legal person responsible for the import and, where applic…
…ation of plasma, whatever its level of processing, which cannot be used as it is for administration to humans, and which is intended for the preparation of health products.
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…
This section applies to plasma pastes and labile blood products intended for the preparation of health products. It also applies to labile blood products for direct therapeutic use included on the lis…
…eisure time and organising sports; 4° Institutions of a professional or educational nature attached to or dependent on the undertaking, such as apprenticeship and vocational training centres, librarie…
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…within fifteen days of receiving the file and by registered letter with acknowledgement of receipt, to send its conclusions within one month..
On receipt of the conclusions referred to in the previous article, the secretary of the commission shall send a copy to the public prosecutor at the Cour de cassation and, by registered letter with ac…
…gement of receipt, within fifteen days of their submission, of the conclusions of the Public Prosecutor at the Court of Cassation and the conclusions of the person referred to in Article R. 40-9. He c…
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