Learning Paths
Core
Build
- CAPA and Effectiveness Checks
- Supplier Quality Management
- Customer Complaint Handling
- Inspection Readiness: Your Role & Preparing for Inspector Interactions
- How to Write Effective Standard Operating Procedures (SOPs)
- ICH Q9 – Quality Risk Management
- Change Control: Core Concepts
- Process Validation: Core Concepts
Refresh
FDA Inspection Readiness (GMP Auditing)
Inspection Readiness: Your Role & Preparing for Inspector Interactions
25 mins
Basic
Good Documentation Practices (GDocP)
How to Write Effective Standard Operating Procedures (SOPs)
60 mins
Basic
International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)
ICH Q9 – Quality Risk Management
25 mins
Intermediate
FDA Inspection Readiness (GMP Auditing)
How Self-Inspection Leads to Continuous Improvement
3 mins
Basic