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Pharmaceutical Quality Control Course

Pharmaceutical Quality Control Course
from 4 to 360h flexible workload
valid certificate in your country

What will I learn?

This course equips you with practical skills to establish and justify specifications for finished products, create sampling plans, and oversee in-process controls for large batches. Master analytical method validation, interpreting borderline results, performing risk-based investigations, managing OOS results, and producing inspection-ready documentation that aligns with FDA, EMA, WHO, USP, and ICH standards.

Elevify advantages

Develop skills

  • Batch release decisions: justify release, hold, or rejection using solid QC data.
  • Regulatory mastery: apply ICH, USP, FDA, EMA, and WHO guidelines to tablet QC.
  • Analytical validation: set up and validate assay, dissolution, and CU methods quickly.
  • Risk-based QC: use FMEA and root cause tools to manage deviations in days.
  • Sampling and IPC: design smart tablet sampling and in-process controls for QA.

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.
Workload: between 4 and 360 hours

What our students say

I was just promoted to Intelligence Advisor for the Prison System, and the course from Elevify was crucial for me to be the chosen one.
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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