GMP (Good Manufacturing Practice) Course
Master Good Manufacturing Practice in pharmaceutical chemistry. Learn compliant cleaning validation, documentation, labelling, in-process controls, environmental monitoring, and deviation/CAPA management. Protect product quality, pass audits, and boost your QA or production career with reliable skills for everyday compliance.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
This GMP course provides practical tools to enhance production quality and compliance. You'll learn to handle cleaning validation, precise record-keeping, safe handovers, ALCOA+ principles, and data integrity. Gain expertise in 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
- GMP documentation mastery: apply ALCOA+ and GDP in production records.
- Cleaning validation skills: qualify equipment, verify results, resolve log issues quickly.
- In-process control expertise: set sampling, assess OOS/OOT, manage deviations.
- Deviation and CAPA handling: investigate root causes, implement robust actions.
- Material and label control: ensure batch traceability, prevent mix-ups.
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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