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Showing 4891–4900 of 27949 articles for “Art. Aut. conc. n° 12-DCC-83 du 13 Jun 2012”
…shments referred to in Article R. 5121-187, the person administering the blood-derived medicinal product to the patient completes the dispensing and administration slip with the following information:…
…drug dependence and addictovigilance assessment and information centres referred to in article R. 5132-112 and the poison control centres referred to in article L. 6141-4 to provide him with any info…
…he Groupement de Coopération Sanitaire, departments may have a supply of blood-derived medicinal products intended for urgent care. This supply is managed in accordance with the provisions of the orde…
I.-The Director General of the Agence nationale de sécurité du médicament et des produits de santé, on the basis of concerns resulting from the evaluation of data from pharmacovigilance activities, in…
In health establishments and health cooperation groups authorised under article L. 6133-7 to carry out the tasks of these establishments which do not have an in-house pharmacy which hold blood-derived…
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…
When the in-house pharmacy dispenses 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 initi…
…for in this paragraph take the place of the transcriptions and recordings mentioned in article R. 5132-10.
When a healthcare professional administers a blood-derived medicinal product outside healthcare establishments or the establishments and organisations mentioned in article R. 5121-192, he/she affixes…
…alth establishments and health cooperation groups authorised to dispense blood-derived medicinal products, these medicinal products are dispensed on the basis of a named medical prescription. When med…
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