Stability Chamber Qualification
Stability Chamber Qualification
Vashishta Engineering Services offers complete validation services for stability chambers, ensuring precise environmental control for pharmaceutical stability studies as per ICH guidelines.
Our Qualification Approach
Mapping Studies
Temperature distribution mapping (+2°C to +40°C)
Humidity uniformity mapping (10-95% RH)
Multi-point mapping for chamber characterization
Empty and loaded chamber studies
Performance Qualification
ICH Q1A compliant validation
Accelerated and long-term condition testing
Photostability testing per ICH Q1B
Power failure and recovery studies
Alarm system verification
Documentation & Compliance
Complete protocol development and execution
Detailed summary reports with data analysis
Audit-ready documentation package
Compliance with WHO, USFDA, and EU GMP requirements