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Clin Pharmacol Ther ; 98(5): 522-33, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26261064

ABSTRACT

Structured frameworks for benefit-risk analysis in drug licensing decisions are being implemented across a number of regulatory agencies worldwide. The aim of these frameworks is to aid the analysis and communication of the benefit-risk assessment throughout the development, evaluation, and supervision of medicines. In this review, authors from regulatory agencies, pharmaceutical companies, and academia share their views on the different frameworks and discuss future directions.


Subject(s)
Communication , Government Agencies/trends , Risk Assessment/trends , United States Food and Drug Administration/trends , Drug-Related Side Effects and Adverse Reactions/diagnosis , Drug-Related Side Effects and Adverse Reactions/epidemiology , Europe , Forecasting , Government Agencies/standards , Humans , Risk Assessment/methods , United States , United States Food and Drug Administration/standards
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