With our stability testing systems, you can perform storage to determine the shelf life of pharmaceutical substances highly safely and in accordance with legal requirements – including monitoring, calibration and qualification. Our spectrum ranges from small test chambers to walk-in stability test chambers and containers that can be used as mobile units to flexibly expand storage capacities. All systems have the necessary documentation capabilities according to FDA 21 CFR Part 11 and EU GMP Annex 11 and comply with ICH guidelines Q1A and Q1B as well as national and international requirements. Benefit from our complete package with documentation, qualification, training options and all necessary services including DAkkS calibration.