Clinical Trials Course
What will I learn?
Improve your clinical trials knowledge with our complete course for health workers. We'll look at the ethics, like getting permission from patients and keeping their information safe. You'll also learn how to plan a trial and write a good plan for it. Understand the different trial stages, how to collect data, and how to analyze it using statistics. We'll also talk about how to handle problems like side effects and when people leave the trial. Our modules are short, good quality, and focus on practical skills so you can do well in clinical research here in Senegal.
Apoia's Unique Features
Develop skills
Enhance the development of the practical skills listed below
Learn the ethical rules: Make sure patients agree to take part and that their information is protected.
Plan strong trials: Create good randomized controlled trials that work well.
Develop good protocols: Write full plans for clinical trials.
Analyze data well: Use statistics and computer programs to understand the data.
Handle problems effectively: Know how to deal with side effects and keep the trial going well.
Suggested overview
Workload: between 4 and 360 hours
Before getting started, you can adjust the chapters and the workload.
- Choose which chapter to begin with
- Add or remove chapters
- Increase or decrease the course workload
Examples of chapters you can include
You'll be able to create more chapters like the examples below
This is a free course, focused on personal and professional growth. It is not equivalent to a technical, undergraduate, or postgraduate course, but offers practical and relevant knowledge for your professional journey.