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Showing 2091–2100 of 38523 articles for “Art. L 228-13”
The presentation, at scientific or technical meetings, exhibitions or demonstrations, of medical devices which do not comply with the provisions of this Title is authorised provided that a visible sig…
The presentation at scientific or technical meetings, exhibitions and demonstrations of in vitro diagnostic medical devices which do not comply with the provisions of this Title is authorised provided…
Every manufacturer of medical devices, or its authorised representative, appoints a material vigilance correspondent and communicates his name to the Director General of the Agence nationale de sécuri…
User healthcare professionals working in one of the establishments mentioned in 4° of Article R. 5222-3 or in a blood transfusion establishment immediately report to the local reactovigilance correspo…
The decisions of the Board of Directors concerning the budget and the financial account are enforceable under the conditions laid down in Title III of Decree no. 2012-1246 of 7 November 2012 on public…
The contract is for a maximum of five years; it may be revised by amendment.
The granting of a nuclear medicine activity authorisation is subject to compliance with the applicable provisions of Chapter III of Title III of Book III of Part One of this Code.
The nuclear medicine authorisation includes one of the following entries: 1° "A" entry, when the activity includes diagnostic or therapeutic procedures, excluding cancer therapy, performed by administ…
I.-An "A" nuclear medicine authorisation may only be granted if the holder has a formalised emergency procedure enabling patients to be cared for if necessary, within a timeframe compatible with healt…
The purpose of home hospital care is to provide continuous, coordinated medical and paramedical care in the patient's own home. This care differs from that usually provided at home in the complexity a…
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