Article R5131-2
…cturing practices mentioned in Article 8 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 concerning cosmetic products. The certificate application is…
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Showing 5301–5310 of 64444 articles for “Art. s. 1341-2 and 2224”
…cturing practices mentioned in Article 8 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 concerning cosmetic products. The certificate application is…
…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…
…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…
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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