Article R5121-181
…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…
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Showing 1211–1220 of 26507 articles for “Art. Loi n° 2014-626 du 18 juin 2014”
…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…
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…
The establishment in which the operations for which authorisation has been granted are carried out operates in compliance with the rules of good practice laid down under the conditions referred to in…
…y way of derogation from the first paragraph of Article R. 5141-16, for the veterinary medicinal products mentioned in this Article, the dossier attached to the marketing authorisation application is…
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