UI Pharmaceuticals Offers a Full Range of Stability Storage Conditions and Testing Options

University of Iowa 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.

Man opening door

The University of Iowa Pharmaceuticals (UIP) Stability Assessment Group has extensive experience performing pharmaceutical stability studies on active pharmaceutical ingredients, early prototype formulations, and finished dosage forms.  In addition, UIP 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)

Stability Testing

Stability testing

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

To learn more about our pharmaceutical stability testing capabilities, please Contact Us or look through our Full Equipment List here.