Discussion on issues in adaptive design for clinical trials with Dr. Deepak L. Bhatt and Dr. Cyrus Mehta Posted on August 18, 2016 by henrykotula • Posted in Uncategorized • Tagged Clinical Outcomes, Clinical Research and Development, Clinical Trials, Clinical Trials Adaptive Design, Ethics, Evidence-based Medicine, Health Policy, Medical Monitors, Operational Bias, Patient Advocacy, Precision Medicine, Regulatory Review, Sample Size Reestimation, Statistical Bias, Statistical Validation • Leave a comment Share this: Click to share on X (Opens in new window) X Click to share on Facebook (Opens in new window) Facebook Click to share on LinkedIn (Opens in new window) LinkedIn Like Loading...
HENRY KOTULA 