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Showing 8291–8300 of 33578 articles for “Art. 3 oct. 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…
If the competent body terminates the appointment of a pharmacist or veterinary surgeon as pharmacist or veterinary surgeon in charge, or refuses to renew the appointment when it expires, the pharmacis…
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 companies mentioned in article R. 5142-1 may export the veterinary medicinal products they sell, transfer free of charge or distribute outside national territory.Exports by these companies to othe…
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.
For the purposes of placing a custom-made medical device on the market, the manufacturer shall follow the procedure defined in Article R. 5211-51. The Director General of the Agence nationale de sécur…
…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…
The content and methods of presentation of the declaration are laid down, on a proposal from the Director General of the Agence nationale de sécurité du médicament et des produits de santé, by order o…
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