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Management of Missing Data in Clinical Trials from a Regulatory Perspective H.M. James Hung

Management of Missing Data in Clinical Trials from a Regulatory Perspective H.M. James Hung Div. of Biometrics I, OB/OPaSS/CDER/FDA Presented in FDA/Industry Workshop, Bethesda, Maryland, September 23, 2004. Collaborators Charles Anello, Yeh-Fong Chen, Kun Jin, Fanhui Kong,

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Obs sample - PowerPoint PPT Presentation

Management of Missing Data in Clinical Trials from a Regulatory Perspective H.M. James Hung