Pharmaceutical Comprehensive Light Stability Test Chamber

Controlled environment system for accelerated and long-term stability testing of pharmaceutical products and medical devices. Ensures compliance with regulatory requirements for drug and device shelf-life validation.

JeioTech Pharmaceutical Stability Test Chamber is a dedicated 400 L system designed to meet ICH Q1A(R2) and ICH Q1B Option 2 requirements (0–70°C, 20–75%RH). Its energy-saving proportional-control refrigeration maintains stable temperature and humidity during long-term testing and keeps conditions consistent regardless of lamp On/Off status. It also supports continuous 5°C long-term testing without defrost interruption, and eases maintenance with in-operation water refilling and a built-in direct water supply connection. For photostability testing, the unit independently controls VIS/UVA light sources and uses an optical sensor to display actual and cumulative illuminance for accurate, compliant testing. A 7-inch color touch controller enables simultaneous control of temperature, humidity, illuminance, and UV, while Level-Checker™ and Multi-Timer™ simplify multi-sample scheduling. Usability and security are enhanced with an inner glass door, key lock, and two cable ports.

Stability testing chamber utilizing Peltier technology to maintain controlled temperature, humidity, and illumination environments. Designed for pharmaceutical product stability testing and drug development studies.

An advanced environmental testing chamber designed to maintain strict temperature and humidity control for pharmaceutical and biological product stability testing. Meets regulatory requirements for long-term storage condition monitoring.

A specialized chamber with semiconductor cooling for pharmaceutical stability testing. Provides controlled temperature and humidity environments meeting pharmaceutical testing standards.

Climatic testing chamber maintaining precise temperature and humidity conditions for stability testing and sample preservation. Critical for pharmaceutical and medical device quality assurance protocols.

Environmental chamber maintaining both temperature and humidity at precise levels for sensitive applications. Suitable for material stability testing and environmental research.

Controlled environmental chamber for accelerated aging studies of medical device materials and components across temperature and humidity ranges. The system simulates long-term storage and use conditions affecting device performance.

Temperature and humidity controlled environmental chamber for testing medical devices and materials. Capable of simulating conditions from -86°C to +250°C for validation and quality assurance purposes.

Environmental test chamber for simulating and testing various temperature conditions ranging from -86°C to +250°C. Utilized for quality control and validation testing of medical devices and materials.

A chamber with semiconductor cooling that maintains precise temperature and humidity control. Used for stability testing and environmental simulation in laboratory settings.

Integrated system for continuous monitoring of contamination, temperature, and humidity in laboratory environments. Enables validation of cleanroom performance and regulatory compliance documentation.