- Biostatistics
- Science and Research
- Informed Consent
- Good Clinical Practices (GCP)
- Clinical Research
- Clinical Research Ethics
- Regulatory Compliance
- Healthcare Ethics
- Clinical Trials
Design and Conduct of Clinical Trials
Completed by Brendan Eck
November 12, 2024
4 hours (approximately)
Brendan Eck's account is verified. Coursera certifies their successful completion of Design and Conduct of Clinical Trials
What you will learn
Evaluate and select clinical trial designs
Implement bias control measures
Randomize participants into groups
Define clinical trial outcomes
Skills you will gain
