Facilities & Equipment

Our facilities are equipped with 17,000 cubic feet of state-of-the-art temperature and humidity-controlled chambers that are continuously monitored and independently alarmed to alert for any environmental changes.

All of our storage environments undergo stringent Installation Qualification (IQ), Operation Qualification (OQ), Performance Qualification (PQ) as well as routine calibration assessments. We regularly invest in capital improvements to ensure all of our test facilities have the latest test technologies and capabilities, and our stability conditions are routinely upgraded to remain current with ICH (International Conference on Harmonization) climatic zones and conditions as well as FDA Guidelines.

Our storage environments include:

• Ultrafreezer NMT -70°C
• Freeze/thaw -20°C to 50°C programmable
• 20°C ± 5°C
• 20°C ± 3°C
• 23°C ± 2°C / 75% RH ± 3% RH*
• 25°C ± 2°C / Ambient Humidity
• 25°C ± 2°C / 40% RH ± 5% RH
• 25°C ± 2°C / 60% RH ± 5% RH
• 30°C ± 2°C / 60% RH ± 5% RH
• 30°C ± 2°C / 65% RH ± 5% RH
• 40°C ± 2°C
• 40°C ± 2°C / NMT 25% RH
• 50°C ± 2°C

* Condition for container permeation testing

Additional temperature and humidity conditions, including Zones I-IV, are also available. Please contact AAIPharma Services for more information or a proposal.