GMP (Good Manufacturing Practice) Course
This GMP course equips you with essential skills in compliant cleaning, documentation, labelling, in-process controls, environmental monitoring, and deviation/CAPA management for pharmaceutical production. Protect product quality, pass audits effortlessly, and elevate your QA or production career with reliable practices.

4 to 360 hours of flexible workload
certificate valid in your country
What Will I Learn?
Gain practical GMP tools to boost production quality and compliance. Master cleaning validation, precise logging, secure handovers, ALCOA+ documentation, data integrity, material labelling, in-process controls, environmental monitoring, and deviation/CAPA processes to minimise errors, ace inspections, and ensure consistent product quality daily.
Elevify Advantages
Develop Skills
- Master GMP documentation using ALCOA+ and GDP for production records.
- Develop cleaning validation skills to qualify equipment and resolve log issues swiftly.
- Gain expertise in in-process controls, sampling, OOS/OOT assessment, and deviation response.
- Learn to handle deviations and CAPA by investigating root causes and implementing strong actions.
- Ensure material and label control for complete batch traceability and mix-up prevention.
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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