Article R5139-26
…rom the Director General of the Agence nationale de sécurité du médicament et des produits de santé and after obtaining the opinion of the Director General of the Agence nationale de sécurité sanitair…
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Showing 5501–5510 of 70142 articles for “Art. 2° and partition duty”
…rom the Director General of the Agence nationale de sécurité du médicament et des produits de santé and after obtaining the opinion of the Director General of the Agence nationale de sécurité sanitair…
…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…
…pharmacists managing pharmacies for internal use, doctors authorised to dispense medicinal products;2° Veterinary surgeons, army veterinary surgeons, and veterinary surgeons or doctors of pharmacy app…
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…
Medical devices must be designed and manufactured, taking into account the generally recognised state of the art, in such a way that, when used in accordance with their intended purpose and under the…
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…
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