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Showing 7501–7510 of 47042 articles for “Art. L 134-4”
For each batch of medicinal products referred to in articles R. 5142-45 and R. 5142-46, the pharmacist or veterinarian responsible shall release the batches and certify that each manufacturing batch c…
Pharmaceutical establishments carrying out one or more of the operations making up the operation must have a documentation system comprising the procedures and records covering the operations they car…
The Agency's inspectors will carry out inspections as decided by the Agency's Director General, who will issue a letter of assignment to the inspector in charge of the investigation. This letter speci…
For Class IIa devices, the authorized body must, as part of the assessment of the quality system, assess the technical documentation for at least one representative sample of each device subcategory i…
For the purposes of the EC declaration of conformity procedure referred to in the first paragraph of Article R. 5211-40 and the EC type-examination procedure referred to in the first paragraph of Arti…
Admission to a national health facility or to a health facility located in an inter-regional directorate of prison services other than the one in which the prisoner is imprisoned must be authorised by…
Prisoners admitted to hospital are considered as continuing to serve their sentence or, in the case of remand prisoners, as being remanded in custody.
When the hospitalisation of a prisoner is required under the conditions referred to in article R. 6111-39, the head of the penitentiary establishment shall notify the director of the health establishm…
Doctors working in prisons are kept informed of changes in the state of health of hospitalised prisoners.
I. - Exceptionally and on a temporary basis, in the absence of available paediatric critical care beds, patients under the age of 18 may be treated in adult critical care on site or by agreement with…
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