Climate chamber

temperaturehumidityfor the pharmaceutical industry

Medicinal products are subject to particularly strict guidelines worldwide. With our stability testing systems, you can determine the shelf life of pharmaceutical substances extremely safely and in accordance with legal requirements. The spectrum ranges from laboratory-scale systems to walk-in climate chambers for optimum long-term testing. All systems have the necessary documentation options according to FDA 21 CFR Part 11 and EU GMP Annex 11 and comply with ICH guidelines Q1A and Q1B. The highly accurate and reliable PharmaEvent stability test chambers are validatable and specifically designed to enable you to meet the requirements of ICH guideline Q1A. Also other national and international requirements such as WHO, FDA, and CPMP are met. The insulating cells can be optimally adapted to the existing building structure because there are no fixed dimensions. The standard height is 2,700 mm; other dimensions are possible. Test chambers and test spaces with a volume of 10–800 m³ are available. Ideal for integration into your building Absolute homogeneity thanks to ideal air flow – even with loaded systems Energy-efficient construction GMP-compliant user management with audit trail and alarm system according to GAMP Operation from the workstation without additional software using the integrated WEBSeason® Multilingual operation Connection to the Simpati pharma monitoring system; can also be integrated into LIMS systems