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Drug Regulatory Affairs Course
Get a good understanding of the important things in drug regulatory affairs with our complete course made just for pharmacy workers. Learn about how drugs get approved according to the ZAMRA (Zambia Medicines Regulatory Authority) process, find out how to make sure everything is followed correctly, and learn your way around the different regulatory rules. Become good at labelling, paperwork, and getting ready to send in regulatory applications. Get better at clinical trials and safety checks while learning how to talk to regulatory groups properly. Make your career better with useful, high-quality knowledge that's made to be used in real life.
- Know the ZAMRA approval stages well: Be able to get drugs approved confidently.
- Make checklists to make sure everything is followed: Make sure you follow the rules properly and easily.
- Understand the regulatory rules: Learn the key rules for medicines.
- Get good at labelling: Meet the standards for paperwork and labelling.
- Plan how to send in regulatory applications: Have a good plan to send in drug applications successfully.

from 4 to 360h flexible workload
certificate recognized by MEC
What will I learn?
Get a good understanding of the important things in drug regulatory affairs with our complete course made just for pharmacy workers. Learn about how drugs get approved according to the ZAMRA (Zambia Medicines Regulatory Authority) process, find out how to make sure everything is followed correctly, and learn your way around the different regulatory rules. Become good at labelling, paperwork, and getting ready to send in regulatory applications. Get better at clinical trials and safety checks while learning how to talk to regulatory groups properly. Make your career better with useful, high-quality knowledge that's made to be used in real life.
Elevify advantages
Develop skills
- Know the ZAMRA approval stages well: Be able to get drugs approved confidently.
- Make checklists to make sure everything is followed: Make sure you follow the rules properly and easily.
- Understand the regulatory rules: Learn the key rules for medicines.
- Get good at labelling: Meet the standards for paperwork and labelling.
- Plan how to send in regulatory applications: Have a good plan to send in drug applications successfully.
Suggested summary
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.What our students say
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