- Clinical Trials
- Clinical Research Ethics
- Healthcare Ethics
- Science and Research
- Biostatistics
- Regulatory Compliance
- Good Clinical Practices (GCP)
- Clinical Research
- Informed Consent
Design and Conduct of Clinical Trials
Completed by SHRUTI SHAH
September 24, 2024
4 hours (approximately)
SHRUTI SHAH'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
