- Biostatistics
- Clinical Research Ethics
- Clinical Trials
- Good Clinical Practices (GCP)
- Informed Consent
- Regulatory Compliance
- Science and Research
- Healthcare Ethics
- Clinical Research
Design and Conduct of Clinical Trials
Completed by Sanjana Hemdev
January 25, 2025
4 hours (approximately)
Sanjana Hemdev'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
