Clinical Trial Design Course
What will I learn?
Get a good grasp of the important parts of designing clinical trials with our course, made especially for healthcare workers here in Zambia. We'll look closely at what's right and wrong when doing research, including making sure people agree to take part (informed consent) and keeping their information private. You'll learn how to pick the best trial design, set clear goals, and follow the rules set by organizations like the Medicines Regulatory Authority in Zambia. You'll also become skilled in using statistics to understand the results, choosing the right people to participate, randomly assigning them to groups, and managing the data properly. This course will give you the skills to run good quality, useful clinical trials that focus on keeping patients safe and making sure the data is accurate.
Apoia's Unique Offerings
Develop your skills
Enhance your practical skills listed below
Uphold ethical standards: Make sure everyone understands and agrees to take part, and keep their information private.
Design effective trials: Choose the best trial design and set clear goals that are achievable.
Understand the regulations: Know the guidelines from the Medicines Regulatory Authority and other important organizations.
Analyze data like a pro: Use statistical methods to get trustworthy results.
Choose the right participants: Calculate how many people you need in your study to get meaningful results.
Suggested summary
Workload: between 4 and 360 hours
Before starting, you can change the chapters and workload.
- Choose which chapter to start with
- Add or remove chapters
- Increase or decrease the course workload
Examples of chapters you can add
You will be able to generate more chapters similar to the examples below
This is a free course aimed at personal and professional development. It is not equivalent to a technical, undergraduate, or postgraduate course, but provides practical and relevant knowledge for your professional journey.