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Interim Analysis in Clinical Trials: A Bayesian Approach in the Regulatory Setting Telba Z. Irony, Ph.D. and Gene Pennello, Ph.D . Division of Biostatistics Office of Surveillance and Biometrics Center for Devices and Radiological Health, FDA

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Interim Analysis in Clinical Trials: A Bayesian Approach in the Regulatory Setting

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Slide1 l.jpg

Interim Analysis in Clinical Trials: A Bayesian Approach in the Regulatory Setting

Telba Z. Irony, Ph.D. and Gene Pennello, Ph.D.

Division of Biostatistics

Office of Surveillance and Biometrics

Center for Devices and Radiological Health, FDA

No official support or endorsement by the Food and Drug Administration of this presentation is intended or should be inferred.


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