The University of Iowa Pharmaceuticals offers a full range of contract pharmaceutical 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 ChamberStability Assessment

The University of Iowa Pharmaceuticals’ (UIP) Stability Assessment Group has extensive experience performing stability studies on active pharmaceutical ingredients, early prototype formulations and finished dosage forms.  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 stability cabinet conditions are continuously monitored with remote notification and have back-up power supply.


For more information about our stability assessment capabilities please Contact Us.


Full Equipment List