Pharmaceutical Quality Assurance Course
Gain mastery in pharmaceutical quality assurance focused on solid oral dosage forms. Delve into GMP practices, batch disposition processes, deviation analysis, corrective actions, and vital quality control methods to safeguard patient health and elevate your expertise in contemporary pharmaceutical production environments. This training equips professionals with essential tools for regulatory adherence and operational excellence.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This course provides hands-on, step-by-step guidance to ensure solid oral dosage batches are safe, compliant, and market-ready. You will gain expertise in manufacturing controls, sampling strategies, GMP standards, deviation management, root cause investigations, CAPA development, and structured decision-making to uphold documentation, meet regulatory demands, and foster ongoing enhancements confidently.
Elevify advantages
Develop skills
- Master control of solid dosage processes including blending, compression, and coating.
- Excel in GMP documentation for batches, deviations, and validation records.
- Investigate deviations and deploy CAPA solutions swiftly and effectively.
- Make informed batch release decisions using QC data, risk assessment, and GMP guidelines.
- Utilise risk-based QA methods like FMEA and data trending for sustained compliance.
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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