GMP (Good Manufacturing Practice) Course
Dive into GMP essentials for pharmaceutical production: master compliant cleaning processes, documentation, labelling, in-process controls, environmental checks, and deviation/CAPA systems. Build skills to safeguard product quality, breeze through inspections, and elevate your career in quality assurance or manufacturing roles.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
This GMP course equips you with practical strategies to boost manufacturing quality and ensure full compliance. Gain expertise in cleaning validation, precise record-keeping, safe shift handovers, ALCOA+ principles for documentation, and data protection. Master labelling materials, in-process checks, environmental monitoring, and handling deviations with CAPA to cut down mistakes, ace audits, and maintain top product standards daily.
Elevify advantages
Develop skills
- Master GMP documentation using ALCOA+ and GDP for accurate production records.
- Develop cleaning validation skills to qualify equipment, confirm results, and resolve log problems swiftly.
- Gain in-process control proficiency: plan sampling, evaluate OOS/OOT results, and manage deviations effectively.
- Learn to handle deviations and CAPA by probing root causes and creating strong corrective plans.
- Ensure material and label management for complete batch tracking 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 workloadWhat our students say
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