- Healthcare Ethics
- Good Clinical Practices (GCP)
- Regulatory Compliance
- Clinical Trials
- Science and Research
- Informed Consent
- Clinical Research
- Biostatistics
- Clinical Research Ethics
Design and Conduct of Clinical Trials
Completed by Kevin De Muynck
June 5, 2024
4 hours (approximately)
Kevin De Muynck'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
