Atlas Pharma Inc. offers its customers the possibility to carry out stability studies of their products, with global storage conditions in accordance with GMP and ICH (International Conference on Harmonisation)
Our storage enclosures validated at temperatures between 25 ° C to 40 ° C and, where appropriate, with humidity control from <60% RH to 75% RH with many options available intermediate.
All stability chambers are monitored by a management system that records temperature and humidity all continuously and notifies appropriate personnel if predetermined 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: