Operate at the specific requirements and exact sizes you need
The primary function of Walk-In Stability Rooms is to offer scalable, reliable environmental regulation, moving beyond the benchtop scale to accommodate palletized or large-equipment testing. Construction is typically custom-tailored to exact specifications, often incorporating insulated panel designs and high-capacity air conditioning systems to maintain specified setpoints precisely, particularly in specialized variants like humidity control rooms, cold rooms above 2℃, and freezers operating down to -30℃. This comprehensive control is essential for validating the storage requirements of sensitive materials and pharmaceuticals.
These rooms are specifically designed to minimize operational vulnerability and the associated financial risk of study failure. Pharmaceutical rooms, for instance, are built with features engineered to actively reduce the potential for losing valuable stability studies, relying on robust, reliable split-system refrigeration and sophisticated redundant control options.
Inconsistent environmental conditions across a large volume are negated by utilizing high-volume air circulation and sophisticated distribution plenums to achieve maximum temperature and humidity uniformity throughout the entire room footprint.
Failure to meet stringent regulatory body requirements (ICH, FDA, TAPPI) is addressed through custom engineering that specifically incorporates features, control methods, and calibration standards necessary to provide auditable and compliant stability storage environments.
The expense and logistical complexity of accommodating large-scale stability studies are solved by these custom-built enclosures, which are configured to the client’s exact volume and layout specifications, minimizing wasted space and optimizing workflow.
Maintaining reliably low temperatures, especially in cold rooms (above 2℃) and freezers (down to -30℃), is ensured by employing innovative split-system refrigeration technology, separating heat-generating components from the controlled environment for enhanced stability and serviceability.
The vulnerability of stability study continuity during component malfunction is minimized by robust system design, incorporating reliable hardware and, optionally, redundant mechanical systems to ensure continuous operation and uninterrupted environmental control.
Material testing applications, particularly in the pulp and paper industry, demand specific conditioning environments; these rooms are custom-built to be TAPPI compliant, ensuring the precise temperature and humidity required for accurate physical property determination.
Rapid or inconsistent thermal recovery after personnel entry or product introduction is controlled by high-capacity conditioning systems sized appropriately for the room volume and expected heat load, ensuring minimal deviation from the specified setpoint.
The long-term cost of operation is managed through superior insulated panel construction, which reduces thermal transfer and minimizes the energy demand on the conditioning units necessary to maintain the precise internal climate over extended stability testing periods.
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