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Showing 3081–3090 of 43824 articles for “Art. 732 & 757 & 758-3 & 758-4”
The President of the Etablissement Français du Sang or the Director of the Armed Forces Blood Transfusion Centre is notified of the decision of the Director General of the Agence Nationale de Sécurité…
I. - Prior written authorisation from the Director General of the Agence nationale de sécurité du médicament et des produits de santé is required for any change to the approval relating to :1° A new t…
Changes other than those subject to authorisation or declaration are described in the annual activity report provided for in article R. 1222-35.
The Director of the Agence nationale de sécurité du médicament et des produits de santé may ask the applicant for any additional information required to examine the application. The request for additi…
I.-The person responsible for the production, distribution or conditioning of water uses, in new installations or parts of installations undergoing renovation, from the point of withdrawal from the re…
I.-Materials and products placed on the market and intended for production, distribution and packaging installations which come into contact with water intended for human consumption must comply with…
In the event of the use of a new technology intended for radiotherapy, radiosurgery, diagnosis or radioguided interventional practices, or of a new type of practice carried out using an existing techn…
I.-In application of 1° of Article L. 1333-2, each category of procedure is justified in general terms under the conditions laid down in Article R. 1333-47. These procedures are carried out when expos…
I.-In liaison with healthcare professionals, the Minister for Health or the body designated by him draws up and distributes a guide defining the medical indications justifying procedures exposing pati…
At the end of the transitional period mentioned in Article R. 1333-48, the information collected and the results of its analysis are taken into account to update the guide provided for in Article R. 1…
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