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Showing 5981–5990 of 58236 articles for “Art. R 418-3 to R 418-7”
The pharmacist must inform the woman concerned that this method of dispensing is non-renewable beyond 6 months and that she should consult a doctor or midwife if she intends to continue taking medicat…
I. - Before issuing the authorisation applied for, the Director General of the Agence nationale de sécurité du médicament et des produits de santé (French National Agency for the Safety of Medicines a…
The certificate is issued by the person responsible for transferring the second-hand medical device to the transferee.
The certificate drawn up by the person responsible for the second-hand resale certifies that the second-hand in vitro diagnostic medical device has been serviced as part of the accreditation referred…
In all cases where the Agency's inspectors identify an infringement likely to result in criminal proceedings, the Agency's Director General will forward the report(s) referred to in Article L. 5411-2…
The Director General of the Regional Health Agency may grant the dispensatory authorisation provided for in Article L. 6122-9-1 to one or more health establishments, with immediate effect and for a pe…
I.- Authorisation for entry 5° under the adult critical care modality and entry 4° under the paediatric critical care modality may only be granted if the holder has an on-site medical unit dedicated t…
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…
The authorisation holder must ensure continuity of care. Through the organisation it puts in place, it guarantees the intervention of a doctor within a timeframe compatible with patient safety. This o…
Authorisation may only be granted if the holder can provide cerebral and vascular exploration by scanner and MRI, on site, twenty-four hours a day, seven days a week.The holder of the medical imaging…
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