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2. Introduction to Systematic Reviews

10. Trials in Minority Populations

11. Introduction to Meta-Analysis

14. De-identifying Clinical Trial Data

16. Publications from Clinical Trials

17. Data Sharing and Reuse

18. Paper Writing

19. Reporting Biases

22. Safety and Risk Benefit Analyses

23. Nonparametric Survival Analysis

24. Bayesian Adaptive Designs for Phase I Trials

25. Estimation and Hypothesis Testing

26. Noninferiority Trials

29. N-of-1 Randomized Trials

30. Diagnostic Trials

31. Sequential, Multiple Assignment, Randomized Trials (SMART)

32. Designs to Detect Disease Modification

33. Cross-over Trials

34. Use of Historical Data in Design

36. Device Trials

37. Randomized Selection Designs

38. Biomarker-Guided Trials

39. Platform Trial Designs

40. Factorial Trials

41. Patient-Reported Outcomes

42. Randomized Discontinuation Trials

43. Within Person Randomized Trials

44. Interim Analysis in Clinical Trials

45. Middle Development Trials

46. Futility Designs

47. Dose-Finding and Dose-Ranging Studies

48. Dose Finding for Drug Combinations

49. Outcomes in Clinical Trials

50. Translational Clinical Trials

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