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Clinical Trial Design Course
Master the ins and outs of clinical trial design with our comprehensive course specifically designed for healthcare professionals. Get stuck into the ethical considerations, including informed consent and participant confidentiality. Learn to choose the right trial design, define clear objectives, and make sure you're complying with regulations from SAHPRA (South African Health Products Regulatory Authority), as well as international guidelines like FDA and EMA. Gain expertise in statistical analysis, participant selection, randomisation, and data management. Equip yourself with the skills to conduct high-quality, effective clinical trials that put patient safety and data integrity first.
- Master ethical standards: Make sure informed consent and confidentiality are sorted.
- Design effective trials: Choose the best designs and set clear objectives.
- Navigate regulations: Get to grips with SAHPRA (South African Health Products Regulatory Authority) guidelines properly.
- Analyse data proficiently: Apply statistical methods for solid conclusions.
- Optimise participant selection: Calculate sample size for significance.

from 4 to 360h flexible workload
certificate recognized by MEC
What will I learn?
Master the ins and outs of clinical trial design with our comprehensive course specifically designed for healthcare professionals. Get stuck into the ethical considerations, including informed consent and participant confidentiality. Learn to choose the right trial design, define clear objectives, and make sure you're complying with regulations from SAHPRA (South African Health Products Regulatory Authority), as well as international guidelines like FDA and EMA. Gain expertise in statistical analysis, participant selection, randomisation, and data management. Equip yourself with the skills to conduct high-quality, effective clinical trials that put patient safety and data integrity first.
Elevify advantages
Develop skills
- Master ethical standards: Make sure informed consent and confidentiality are sorted.
- Design effective trials: Choose the best designs and set clear objectives.
- Navigate regulations: Get to grips with SAHPRA (South African Health Products Regulatory Authority) guidelines properly.
- Analyse data proficiently: Apply statistical methods for solid conclusions.
- Optimise participant selection: Calculate sample size for significance.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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