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Showing 8651–8660 of 18437 articles for “Art. 5 sept. 2012”
…e pharmacy which hold blood-derived medicinal products under the conditions mentioned in article L. 5126-6, the supply of blood-derived medicinal products gives rise to the recording by the correspond…
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…
…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 commiss…
…d for in this paragraph take the place of the transcriptions and recordings mentioned in article R. 5132-10.
…t 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 to…
…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 com…
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…
…4° The date of supply and, for blood-derived medicinal products mentioned in b of 18° of Article L. 5121-1, the time of thawing;5° The quantities dispensed.In the event of a handwritten record, the de…
…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 ou…
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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