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