Stability Chambers “Walk-in” – Aralab

Advanced Stability Testing Rooms for Precise Environmental Control

Aralab Stability ‘walk-in’ chambers for stability testing and controlled environment storage offer unsurpassed stability and uniformity in reproducing temperature and humidity conditions. These environmental chambers are designed to meet the most demanding quality standards for pharmaceutical, cosmetics, food & beverages, and quality control applications.

ICH Q1A Compliant Solutions

Meeting ICH Q1A standards for temperature and humidity stability testing, these chambers come equipped with FDA 21 CFR part 11 software for data logging, and IQ, OQ and PQ (Installation Qualification, Operation Qualification and Performance Qualification) documentation. All stability product range is compliant with ICH Q1A and Q1B Guidelines, ensuring regulatory compliance for pharmaceutical applications.

Flexible Sizing and Customization

Aralab Stability controlled environment rooms are available in an array of sizes, with volumes ranging from 5m³ to 25m³. Additionally, tailor-made solutions are provided to ensure the optimal fit for specific customer needs in terms of footprint and storage capacity. Walk-in stability chambers are designed for high-volume testing and can accommodate extensive product samples.

Advanced Control and Monitoring

Equipped with the exclusive ClimaPlus controller featuring an easy-to-use touch-screen interface with 168mm x 112mm multicolor display. The system controls every environmental variable and includes a friendly program editor for creating 32 programs of 24 segments each, allowing the design of complex and comprehensive climatic simulation programs.

Technical Specifications

  • Volume Range: 5m³ to 25m³
  • Temperature Range: 15°C to 45°C (±1°C uniformity)
  • Humidity Range: 35% to 90% rH (±2.5% uniformity)
  • Temperature extension available to 0°C or negative ranges
  • Construction: EN 14509 sandwich type high density injected polyurethane foam modular panels, 80mm thick
  • Exterior: Galvanized steel in light gray plastic finish
  • Controller: ClimaPlus touchscreen controller (168mm x 112mm multicolor display)
  • Compliance: ICH Q1A and Q1B Guidelines
  • Data Logging: FDA 21 CFR part 11 compliant
  • Documentation: IQ, OQ, PQ qualifications included
  • Calibration: ISO 17025 calibration available

FAQ - Stability Chambers “Walk-in” – Aralab

What are the main applications for Aralab Stability Testing Rooms?

These chambers are ideal for ICH stability testing, pharmaceutical stability studies, food and beverage testing, cosmetics quality control, veterinary storage and conservation, and general quality control and research applications requiring precise environmental conditions.

What volume sizes are available for the stability testing rooms?

Aralab Stability controlled environment rooms are available in volumes ranging from 5m³ to 25m³. Additionally, tailor-made solutions can be provided to ensure the optimal fit for specific customer needs in terms of footprint and storage capacity.

Are these chambers compliant with pharmaceutical regulations?

Yes, all Aralab stability chambers meet ICH Q1A standards for temperature and humidity stability testing, and come with FDA 21 CFR part 11 compliant software for data logging. IQ, OQ and PQ documentation is included for mandatory quality qualifications.

What temperature and humidity ranges can these chambers maintain?

The chambers provide precise control with a temperature range of 15°C to 45°C with ±1°C uniformity, and a humidity range of 35% to 90% rH with ±2.5% uniformity. Temperature extension is available to 0°C or even negative ranges if required.

What type of controller and monitoring system is included?

The chambers are equipped with the exclusive ClimaPlus controller featuring an easy-to-use touch-screen interface with a 168mm x 112mm multicolor display. The system includes a program editor for creating 32 programs of 24 segments each, password protection, and comprehensive alarm systems.

Is data logging and documentation provided?

Yes, the chambers include FitoLog software pack for data monitoring and logging that is FDA 21 CFR part 11 compliant. IQ, OQ, PQ validations and documentation are provided, along with ISO 17025 calibration to validate the exceptional uniformity and stability of conditions.

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