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Réglementation des médicaments au Pakistan

Réglementation des médicaments au Pakistan

Aqeel Nasim / Gullab Khan Kakar / Noman Ul Haq

63,53 €
IVA incluido
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Editorial:
KS OmniScriptum Publishing
Año de edición:
2024
Materia
Farmacología
ISBN:
9786208099527
63,53 €
IVA incluido
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Sobre IBD

La réglementation des produits pharmaceutiques et des médicaments existe depuis le début du 20e siècle. La réglementation et les lois sur les médicaments sont reconnues dans de nombreux pays à travers le monde. Les pays qui disposent d’une organisation réglementaire tentent de s’harmoniser avec elle. Au Pakistan, les industries pharmaceutiques produisent toutes les principales formes de dosage pharmaceutique ; la plupart des matières premières sont importées et certaines sont fabriquées localement. Même si les dépenses totales en médicaments ne sont pas énormes, l’accessibilité à des médicaments sûrs et efficaces reste un problème sérieux. Au Pakistan, l’autorité de régulation des médicaments du Pakistan (DRAP) a été reconnue en vertu de la loi (DRAP) de 2012 pour assurer l’application de la loi sur les médicaments de 1976 et une coordination efficace. Elle a également harmonisé les bonnes pratiques thérapeutiques dans les échanges et le commerce interprovincial. Il fournit une réglementation pour la fabrication, l’exportation, l’importation, le stockage, la vente et la distribution de produits thérapeutiques/pharmaceutiques.

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