European Perspective on Risk Management and Drug Safety

European Perspective on Risk Management and Drug Safety

Risk management is an approach that has been used for many years in areas of business and government such as finance and insurance, but its use in the regulation of medicines has until recently been limited to tools such as the prescription status of a medicine (prescription‐only or over‐the‐counter...

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Veröffentlicht in:Clinical pharmacology and therapeutics 2011-05, Vol.89 (5), p.650-654
Hauptverfasser: Raine, J, Wise, L, Blackburn, S, Eichler, H‐G, Breckenridge, A
Format: Artikel
Sprache:eng
Schlagworte:
Clinical Trials, Phase III as Topic - standards
Clinical Trials, Phase III as Topic - trends
Drug-Related Side Effects and Adverse Reactions
Europe
European Union
Humans
Pharmaceutical Preparations - standards
Risk Management - methods
Risk Management - standards
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Beschreibung
Zusammenfassung:Risk management is an approach that has been used for many years in areas of business and government such as finance and insurance, but its use in the regulation of medicines has until recently been limited to tools such as the prescription status of a medicine (prescription‐only or over‐the‐counter), the information provided to health‐care professionals and patients, and the collection and evaluation of postmarketing safety reports. Clinical Pharmacology & Therapeutics (2011) 89 5, 650–654. doi:10.1038/clpt.2011.28
ISSN:0009-9236
1532-6535
DOI:10.1038/clpt.2011.28