#
Title
1

Episode 62: Drug Adherence and Persistence

2

Episode 61: The Role of Data Monitoring Committees (DMC) in Clinical Trials

3

Episode 60: Oncology Phase 1 Trial Design

4

Episode 59: Clinical Data Quality

5

Episode 58: Rescue Studies

6

Episode 57: Clinical Trial Performance Metrics

7

Episode 56: Bayesian Clinical Trial Design

8

Episode 55: What is Adaptive Trial Design?

9

Episode 54: SAS vs R vs Python in Clinical Trials

10

Episode 53: Decentralised Clinical Trials

11

Episode 52: The Global Statistical Test for Multiple Endpoint Analysis

12

Episode 51: CDASH Standards and Conformance in Clinical Data Management

13

Episode 50: Multi-Omics Application in Personalised Medicine Studies

14

Episode 49: BIMO Listings

15

Episode 48: Efficacy Endpoints in Oncology Clinical Trials

16

Episode 47: The Creation of ADaM Datasets for PK Analysis

17

Episode 46: What is Clinical Data Review?

18

Episode 45: Clinical Trial Management Systems (CTMS)

19

Episode 44: Clinical Trial Simulation

20

Episode 43: Clinical Study Start Up

21

Episode 42: Medical Device Clinical Trials

22

Episode 41: What Are SAD MAD Studies?

23

Episode 40: Functional Service Provision (FSP)

24

Episode 39: Automation in Clinical Trials

25

Episode 38: Observational Studies in Clinical Trials

26

Episode 37: Phase 2b in Clinical Trials

27

Episode 36: ACR Response Criteria in Rheumatoid Arthritis Trials

28

Episode 35: Regulatory Submissions in Clinical Trials

29

Episode 34: Therapeutic Areas in Clinical Research

30

Episode 33: eCRF Design in Clinical Trials

31

Episode 32: Risk-Based Quality Management in CDM

32

Episode 31: Investigator's Brochure (IB)

33

Episode 30: Adaptive Randomisation in Clinical Trials

34

Episode 29: What is Clinical Data Management?

35

Episode 28: Real World Data Analysis in Clinical Trials

36

Episode 27: Machine Learning in the Pharmaceutical Industry

37

Episode 26: Medical Coding in Clinical Data Management

38

Episode 25: The Proportional Odds Assumption in Clinical Trials

39

Episode 24: Health Economics and Outcomes Research (HEOR)

40

Episode 23: Query Management in Clinical Trials

41

Episode 22: Quality Tolerance Limits in Clinical Trials

42

Episode 21: The Role of Reconciliation in Clinical Data Management

43

Episode 20: Missing Data in Clinical Trials

44

Episode 19: Data Validation in Clinical Data Management

45

Episode 18: Real World Evidence in Clinical Trials

46

Episode 17: Dose Expansion Phases in Oncology Trials

47

Episode 16: Statistical Analysis Plans (SAPs)

48

Episode 15: CRF Annotation in Clinical Trials

49

Episode 14: Using R Programming for Clinical Trial Data Analysis

50

Episode 13: Estimands in Clinical Trials

51

Episode 12: AI and Automation in Clinical Data Management

52

Episode 11: A Guide to Virtual Clinical Trials

53

Episode 10: Managing Clinical Data Challenges with a DSMB

54

Episode 9: Randomisation in Clinical Trials

55

Episode 8: The Database Lock Process in Clinical Trials

56

Episode 7: A Guide to Phase 1 Clinical Trial Designs

57

Episode 6: The ALCOA++ Principles for Data Integrity in Clinical Trials

58

Episode 5: CDISC Standards in Clinical Research

59

Episode 4: BOIN Design in Clinical Trials

60

Episode 3: Complex Innovative Trial Designs

61

Episode 2: Guide to Integrated Summaries of Safety and Effectiveness

62

Episode 1: The Use of Wearables in Clinical Trials