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Activity Details

63 * ! Sun, 8/3/2014, 4:00 PM - 5:50 PM CC-260
Missing Data in Safety Evaluation and Observational Studies — Topic Contributed Papers
Biopharmaceutical Section
Organizer(s): Freda Cooner, FDA/CDER
Chair(s): Freda Cooner, FDA/CDER   
4:05 PM Missing Data in Safety Evaluation: Experiences and Case Examples Aloka Chakravarty, FDA
4:25 PM Minimizing Missing Data in the Design of Observational Clinical Studies Lilly Yue, FDA/CDRH
4:45 PM Discussant: Peter Mesenbrink, Novartis
5:05 PM Discussant: Chenguang Wang, Johns Hopkins Medicine
5:25 PM Floor Discussion

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