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Showing 8341–8350 of 47428 articles for “Art. 3 mai 2007”
The natural or legal person who initiates a veterinary medicinal product trial as defined in article R. 5141-2 is called the sponsor. The persons who direct and supervise the performance of pharmaceut…
Pharmacists and veterinary surgeons who assist the pharmacist or veterinary surgeon in charge are known as assistant pharmacists and veterinary surgeons. They are registered respectively in section B,…
The company sends the Director General of the Agence nationale de sécurité sanitaire de l'alimentation, de l'environnement et du travail a copy of any document appointing the pharmacist or veterinaria…
As part of the EC declaration of conformity procedure, the manufacturer shall draw up technical documentation making it possible to assess the conformity of the medical device with the essential requi…
For medical devices to be subject to clinical investigations, the manufacturer must comply with the provisions of Title II of Book I of Part I of this Code.
…e quality control has led to the reporting of a risk of incident as provided for in Article R. 5212-31, the operator shall notify the Director General of the Agence nationale de sécurité du médicament…
…cond quality control carried out on the device in accordance with the provisions of Article R. 5212-30.If, after this second inspection, the expected performance of the device is still not achieved, t…
…n Articles R. 5212-27 and R. 5212-27-1. Each external quality control gives rise to a report on the maintenance of the performance of the device inspected. This report mentions the name of the operato…
…gal representative of health establishments, health cooperation groupings mentioned in article L. 6133-7 and cosmetic surgery establishments shall, after consulting the medical committee of the establ…
For medical devices, the list of which is set by order of the Minister for Health on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé (Fr…
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