Our qualification services cover the full validation lifecycle for computerized systems in regulated pharmaceutical environments. We ensure your systems meet IQ, OQ, and PQ requirements with comprehensive documentation and regulatory compliance.
Installation Qualification (IQ)
- System installation verification
- Configuration documentation
- Hardware/software inventory
Operational Qualification (OQ)
- Functional testing
- Boundary condition testing
- Test script execution
Performance Qualification (PQ)
- Real-world process simulation
- User acceptance testing
- Performance benchmarking
Validation Documentation
- Validation master plan
- Protocol development
- Summary reports