- 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 Farah Omran
March 18, 2024
4 hours (approximately)
Farah Omran'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
