Whether your testing is for R&D, clinical trials or ongoing stability, the TEMPO stability chamber provide a stable temperature & humidity condition environment for worry-free operations with a control system that is easy to operate. TEMPO make stability chamber is designed as per ICH guidelines and are manufactured to comply with requirements in the industries. Stability testing is an integral part of formulation development. It helps to generate information, which permits well-considered proposals to be made for the shelf life of drug substances and products and recommended storage conditions. The purpose of stability testing is to provide evidence on how the quality of a drug substance or drug product varies with time under the influence of a variety of environmental factors such as temperature, humidity, and light, and to establish a re-test period for the drug substance or product under recommended storage conditions. Hence, the pharmaceutical stability chamber serves as an important quality attribute for the product. Temperature range 20 C to 60 C Temperature accuracy �±0.2 C Temperature uniformity �±1 C Humidity Range 40% Rh to 90% Rh Humidity Accuracy �±2%Rh Humidity Uniformity �±3%Rh Technical Specification Controlling System Two separate imported microprocessors based auto tune PID controller with CE mark & dual display of set value & process value for temperature & humidity with direct %RH. Air Circulation The motorized blower at the backside of the chamber develops a unique air ow system which ensures max. uniform temperature & humidity condition inside the chamber. Heating System High-quality U shape S.S. tubular heater is used for better heating. Humidity System Steam injection system (Non-condensing type) & reservoir tank with water level arrangement with indicator. Refrigeration System CFC Free hermetically sealed Emerson Copeland make compressor for better cooling with R134 A (Eco Friendly) refrigerant with a time delay to safeguard compressor system.
