GMP (Good Manufacturing Practice) Course
Gain mastery in GMP for pharmaceutical production: cover compliant cleaning validation, documentation with ALCOA+ and GDP, labelling controls, in-process checks, environmental monitoring, and deviation/CAPA handling. This equips you to safeguard product quality, pass regulatory audits effortlessly, and elevate your career in quality assurance or manufacturing roles.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This GMP course provides practical tools to boost production quality and compliance. You will learn cleaning validation management, accurate record-keeping, secure handovers, ALCOA+ principles for documentation, data integrity protection, material labelling, in-process controls, environmental monitoring, and deviation/CAPA processes to cut errors, ace inspections, and ensure consistent product quality daily.
Elevify advantages
Develop skills
- Master GMP documentation using ALCOA+ and GDP for production records.
- Develop skills in cleaning validation to qualify equipment and resolve log issues quickly.
- Build expertise in in-process controls including sampling, OOS/OOT assessment, and deviation response.
- Learn to handle deviations and CAPA by investigating root causes and implementing strong corrective actions.
- Ensure material and label control for complete batch traceability and mix-up prevention.
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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