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Showing 3561–3570 of 44727 articles for “Art. 1873-3 · C. civ. Art. 1873-4”
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…
…and the potential exposure of professionals involved in carrying out the procedures and of the public.II-The assessment of the justification takes into account, in particular:1° The effectiveness, ben…
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…
The body referred to in Article L. 8252-4 is the French Office for Immigration and Integration.
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