UI Pharmaceuticals

Stability Assessment

Stability Assessment

UI Pharmaceuticals stability cabinets are monitored 24/7. Not only are we able to perform routine stability assessments, but we also routinely perform shorter duration in-use and reconstituted stability studies.  Let us help you meet your stability storage and testing needs.

The UI Pharmaceuticals Stability Assessment Group has extensive experience performing pharmaceutical stability studies on active pharmaceutical ingredients, early prototype formulations, and finished dosage forms.In addition, UI Pharmaceuticals routinely performs specialized reconstituted, freeze/thaw cycling, and in-use stability assessments.

Pharmaceutical stability testing is performed according to FDA-ICH guidelines, client-approved protocols, and standard operating procedures.

Available stability storage conditions include:

• -80ºC
• -20ºC
• 2 to 8ºC
• 25ºC/60% RH
• 30ºC/65% RH
• 40ºC/75% RH
• Xenon-arc Light Cabinet
• Customized Conditions (such as freeze/thaw cycling)

All drug stability cabinet conditions are continuously monitored with remote notification and have a backup power supply.