Pharmaceutical Quality Assurance Course
Gain expertise in quality assurance for solid oral dosage forms in pharmaceuticals. Delve into GMP practices, batch disposition processes, handling deviations, CAPA systems, and vital QC techniques to safeguard patient health and elevate your contribution in contemporary drug production environments. This comprehensive program equips you with essential skills for regulatory compliance and operational excellence.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
This course offers hands-on training to ensure safe, compliant solid oral dosage batches ready for market. Master manufacturing controls, sampling strategies, GMP standards, deviation management, root cause investigations, CAPA implementation, and decision-making protocols for strong documentation, regulatory adherence, and ongoing enhancements.
Elevify advantages
Develop skills
- Master controls for blending, compression, and coating in solid dosage production.
- Excel in GMP documentation for batches, deviations, and validation reports.
- Investigate deviations and deploy CAPA solutions swiftly and effectively.
- Make informed batch release choices using QC data, risk assessment, and GMP guidelines.
- Utilise risk tools like FMEA and data trending for sustained compliance.
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.What our students say
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