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Showing 7891–7900 of 39773 articles for “Art. R. 145-5”
…od-derived medicinal products gives rise to the recording by the correspondent mentioned in article R. 5121-181, in a special register marked and initialled by the mayor or by the police commissioner,…
The registers or records provided for in articles R. 5121-185 to R. 5121-193 are kept for a period of forty years. Where necessary for the purposes of pharmacovigilance, the regional pharmacovigilance…
…ses a blood-derived medicinal product directly to a patient, the information referred to in article R. 5121-187 is transcribed onto a special register marked and initialled by the mayor or police comm…
…ided for in this paragraph take the place of the transcriptions and recordings mentioned in article R. 5132-10.
…duct outside healthcare establishments or the establishments and organisations mentioned in article R. 5121-192, he/she affixes a detachable label from the immediate packaging of the unit administered…
…a named medical prescription. When medicines are dispensed, the information referred to in article R. 5121-187 is recorded in a special register which is listed and initialled by the mayor or police…
Pharmacovigilance of blood-derived medicinal products involves monitoring, known as traceability, from the time they are manufactured until they are administered to patients. The purpose of this monit…
In healthcare establishments and other establishments with an in-house pharmacy, blood-derived medicinal products are dispensed by the in-house pharmacy on the basis of a medical prescription.The in-h…
…a blood-derived medicinal product must immediately transcribe the information mentioned in article R. 5132-10, the patient's date of birth and the information appearing on the detachable label of the…
A pharmaceutical establishment manufacturing, operating, importing, exporting or wholesaling blood-derived medicinal products must, when disposing of these medicinal products, record :1° The name, str…
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