The University of Iowa Pharmaceuticals offers a full range of pharmaceutical stability testing services. Let us help you meet your needs.


Stability Assessment

Lyophilization Cycle Development


Clinical Supply Manufacturing


Small Scale Commercial Manufacturing


Analytical Method Development and Validation


Routine Quality Control Analysis


Stability Assessment


Formulation Development


Comparator Products


Powder in a Bottle


Preformulation Studies


Active Pharmaceutical Ingredient (API) and Excipient Release Testing


QP Release Services


Checking Stability ChamberPharmaceutical Stability Testing

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


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


Available stability storage conditions include: Taring Weigh Pan

  • -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)




Reference Standard Storage ChamberAll drug stability cabinet conditions are continuously monitored with remote notification and have back-up power supply.


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