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.