Atlas Pharma Inc. offers its clients the opportunity to conduct stability studies and product durability analyses under global storage conditions that comply with GMP and ICH (International Council for Harmonisation) guidelines.

Our validated storage chambers operate at temperatures ranging from 25 °C to 40 °C and, when required, with controlled humidity levels from <60% RH to 75% RH, with multiple intermediate options available.

All stability chambers are monitored by a management system that continuously records temperature and humidity and alerts the appropriate personnel when predefined alarm criteria are met.

Atlas Pharma Inc. has an experienced staff that can provide a range of stability testing services, including routine testing. See our full range of stability program below: