Article R5121-189
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…
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Showing 1211–1220 of 27836 articles for “Art. Décret n° 2021-300 du 18 mars 2021”
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…
…armacy is the correspondent of the regional pharmacovigilance centre for blood-derived medicinal products. When an establishment has several internal-use pharmacies, the pharmacist managing each of th…
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…
Dispensing pharmacists who dispense 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 appea…
…ablishment manufacturing, operating, importing, exporting or wholesaling blood-derived medicinal products must, when disposing of these medicinal products, record :1° The name, strength and pharmaceut…
…ce not carrying out import activities, practical experience within the health supply establishments during the period prior to the granting of authorisations to open the said establishments is taken i…
The provisions of sections 1 to 3 of this chapter, with the exception of article R. 5122-17, are applicable to advertising for the generators, kits and precursors defined in 8°, 9° and 10° of article…
A full pharmacist may only hold direct or indirect shareholdings in four sociétés d'exercice libéral de pharmaciens d'officine other than the one within which he practises. Subject to the ceiling set…
The provisions of this section apply to the in-house pharmacies of the establishments, services or organisations mentioned in 1°, 2°, 3° and 4° of article R. 5126-1.
…Registration number ; 3° Posology and instructions for use.The label is white when the medicinal product is intended for the nasal, oral, perlingual, sublingual, rectal, vaginal or urethral route or i…
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