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Pharmaceutical Quality Control Course

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

What will I learn?

This course provides hands-on skills for establishing and justifying finished product specifications, creating sampling plans, and overseeing in-process controls for large-scale batches. You will learn to validate analytical methods, analyse borderline results, perform risk-based investigations, address out-of-specification results, and produce inspection-ready documentation compliant with FDA, EMA, WHO, USP, and ICH requirements.

Elevify advantages

Develop skills

  • Batch release decisions: justify release, hold, or rejection using robust QC data.
  • Regulatory mastery: apply ICH, USP, FDA, EMA, and WHO guidelines to tablet QC.
  • Analytical validation: establish and validate assay, dissolution, and CU methods efficiently.
  • Risk-based QC: employ FMEA and root cause analysis to resolve deviations swiftly.
  • Sampling and IPC: develop effective 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 I work for.
SilviaNurse
Really great course. Lots of valuable information.
WiltonCivil Firefighter

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