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