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