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


Routine Quality Control Analysis

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


Water KF TitratorRoutine Quality Control Analysis

The University of Iowa Pharmaceuticals’ (UIP) Quality Control Laboratory has extensive experience performing analyses of in-process and finished product samples, as well as rinse or swab samples to verify cleanliness of manufacturing equipment. 




Tests routinely performed include chemical assay, identification, related substances or impurities, chiral purity, uniformity of dosage forms by weight variation or chemical assay, dissolution, disintegration, appearance, capsule closure, hardness and friability of tablets, dimensions of tablets or capsules, water content, pH, osmolality, viscosity, and instrumental color measurements of drug substances or drug products. 


Programming an HPLCFor more information about our routine quality control testing capabilities please Contact Us.

Full Equipment List