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Showing 5111–5120 of 59269 articles for “Art. D 312-16 and D 312-17”
The authorisation holder ensures that data from professional practices is collected and analysed with the aim of improving practices and risk management.
The holder of the interventional radiology authorisation must ensure that the equipment exposing patients to ionising radiation has the tools required to optimise radiation protection for patients and…
I.-The patient's pathway is organised from the moment they are admitted, the radiology-guided interventional procedure is carried out and the patient is cared for until they are discharged. II-When th…
The authorisation holder must ensure that the equipment is connected to a system for archiving and sharing images in order to improve the quality of care and the relevance of the procedures performed.
Applications for authorisation may only be examined if they are accompanied by a complete file. The application is deemed to be complete if, within one month of receipt, the Minister for Health has no…
The head of the medical biology laboratory established in another Member State of the European Union or party to the Agreement on the European Economic Area shall inform the Minister responsible for h…
The Minister for Health shall maintain and make available to the public a register of laboratories that have made the declaration provided for in the second paragraph of Article L. 6211-2-1 as it stoo…
The declaration provided for in the second paragraph of Article L. 6211-2-1, as it stood prior to the entry into force of amended Order No. 2010-49 of 13 January 2010 relating to medical biology, shal…
When a medical biology laboratory established in another Member State of the European Union or party to the Agreement on the European Economic Area and appearing on a list established by order of the…
The biological samples sent by the medical biology laboratory established in France requesting the analytical phase must be subject to a monitoring procedure to establish the conformity of the biologi…
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