Article R5132-21
A prescription for medicinal products in lists I and II may not be made for a treatment period of more than twelve months.However, for public health reasons, in the case of certain medicinal products,…
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Showing 1561–1570 of 7048 articles for “Art. n° 21-13.970 FS-B”
A prescription for medicinal products in lists I and II may not be made for a treatment period of more than twelve months.However, for public health reasons, in the case of certain medicinal products,…
The production, manufacture, transport, import, export, possession, offer, transfer, acquisition and use of micro-organisms and toxins or products containing them in a form or under a name liable to c…
When an application for authorisation concerns a generic veterinary medicinal product of a reference veterinary medicinal product which has not been authorised in France but which has been authorised…
Medical devices must be designed and manufactured, taking into account the generally recognised state of the art, in such a way that, when used in accordance with their intended purpose and under the…
The in vitro diagnostic medical devices referred to in Article L. 5221-5 may be exempted from conformity assessment procedures only if the procedure corresponding to the category of device does not in…
Without prejudice to the obligations to provide information laid down by Article L. 5212-2 or by any other legislative or regulatory provision, the staff of the Agence nationale de sécurité du médicam…
Failure to make the information provided for in I and II of article L. 5232-5 available to the public under the conditions defined in article R. 5232-20 is punishable by a fifth-class fine. Failure to…
The director, the administrator of the health cooperation group or the legal representative of the establishment defines, on a proposal from the chairman of the establishment's medical commission or t…
The national committee draws up its own rules of procedure, which are submitted to the ministers responsible for social action, health and social security for approval.
The health care organisation organises the coordination of patient care between the emergency department and the other acute care or follow-up departments in the health care organisation if it has one…
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