Clinical Trial Design Course
What will I learn?
Jifunze (Learn) the key things about designing clinical trials with our in-depth course made for Kenyan healthcare workers. We'll look closely at ethical things like getting informed consent and keeping participant information private. You'll learn how to pick the right trial design, make clear goals, and follow rules from places like the FDA and EMA. You'll also become good at statistical analysis, choosing participants, randomization, and managing data. Get the skills you need to run quality clinical trials that focus on patient safety and correct data.
Apoia's Unique Benefits
Develop skills
Enhance your practical skills listed below
Understand ethical rules: Make sure people give informed consent and their information is private.
Design trials that work: Pick the best designs and set clear goals.
Know the regulations: Understand the FDA and EMA guidelines well.
Analyze data like a pro: Use statistical methods to get correct results.
Choose the right participants: Calculate how many people you need for good results.
Suggested summary
Workload: between 4 and 360 hours
Before starting, you can change chapters and the 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 like the examples below
This is a free course, focused on personal and professional development. It does not equate to a technical, undergraduate, or postgraduate course, but offers practical and relevant knowledge for your professional journey.