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Showing 3051–3060 of 54038 articles for “Art. D 230-1”
Any importation of a labile blood product or a plasma paste is subject to prior authorisation issued by the Director General of the Agence nationale de sécurité du médicament et des produits de santé.…
The application for an import authorisation must include : a) The name and address of the importer ; b) The nature and quantity of the product being imported; c) Where applicable, the name and address…
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…
A plasma paste is any intermediate product resulting from the fractionation of plasma, whatever its level of processing, which cannot be used as it is for administration to humans, and which is intend…
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…
The number of judges and the number of chambers in each commercial court are set in accordance with the tables in Annex 7-2 to this book.
The seat and jurisdiction of the commercial courts are determined in accordance with the table in the Annex 7-1 of this book.
The failure to fulfil the training obligation provided for in article L. 722-17 and the date of cessation of duties are recorded by the first president of the court of appeal. The first president of t…
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