- Healthcare Ethics
- Informed Consent
- Regulatory Compliance
- Clinical Trials
- Clinical Research Ethics
- Clinical Research
- Good Clinical Practices (GCP)
- Biostatistics
- Science and Research
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
