- Informed Consent
- Clinical Research Ethics
- Clinical Research
- Science and Research
- Biostatistics
- Healthcare Ethics
- Regulatory Compliance
- Clinical Trials
- Good Clinical Practices (GCP)
Design and Conduct of Clinical Trials
Completed by A G Shashank
January 2, 2024
4 hours (approximately)
A G Shashank '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
