Article R5139-29
…organisms or toxins are prescribed in accordance with the conditions set out in articles R. 5132-3 and R. 5132-4. A prescription may not be made for a treatment period exceeding twelve months. II - P…
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Showing 8711–8720 of 65175 articles for “Art. 1397 al. 9 and Art. 1341-2”
…organisms or toxins are prescribed in accordance with the conditions set out in articles R. 5132-3 and R. 5132-4. A prescription may not be made for a treatment period exceeding twelve months. II - P…
…doctors authorised to dispense medicinal products;2° Veterinary surgeons, army veterinary surgeons, and veterinary surgeons or doctors of pharmacy appointed by the director of the French veterinary sc…
The prescription and supply of medicinal products containing micro-organisms or toxins other than those included on the list provided for in article R. 5139-26 is prohibited. The preparation of any pr…
In order to comply with the essential requirements relating to design and manufacture, active implantable medical devices must be designed, manufactured and packaged in such a way as to meet the follo…
In order to comply with the essential requirements relating to design and manufacture, medical devices, other than active implantable devices, must be designed, manufactured and packaged in such a way…
The conditions for implementing the essential requirements defined in this section are specified, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produ…
…rt of an incident or risk of incident caused by medical devices used in the collection, manufacture and administration of blood-derived products;2° Informing the manufacturers concerned of the inciden…
The operator must ensure that the maintenance and quality controls required for the medical devices it operates are carried out. Maintenance is carried out either by the manufacturer or under his resp…
…ep a regularly updated inventory of the devices it operates, mentioning for each of them the common and commercial names of the device, the name of its manufacturer and that of the supplier, the seria…
…another Member State of the European Union or party to the Agreement on the European Economic Area and having been controlled by a laboratory designated for this purpose by that State. This inspectio…
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