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Drug Regulatory Affairs Course

Drug Regulatory Affairs Course
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.
Workload: between 4 and 360 hours

What our students say

I was just promoted to Intelligence Advisor of the Prison System, and the course from Elevify was crucial for me to be chosen.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company where I work.
SilviaNurse
Very great course. Lots of rich information.
WiltonCivil Firefighter

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