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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

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