Our Commitment to Quality
UI Pharmaceuticals has a rigorous pharmaceutical quality assurance program designed to ensure that FDA Good Manufacturing Practices and European Medicines Agency (EMA) GMP requirements are met. We are routinely inspected by FDA for compliance with cGMP regulations, with our last inspection occurring in the summer of 2023.
Our Commitment to Quality
QP Release Services
The University of Iowa Pharmaceuticals (UIP) has a QP available to sponsors wishing to obtain QP release for their products for clinical trials in the European Union.
Along with QP certification, UIP has experience across the full range of CMC related activities associated with the development; manufacturing (both clinical and commercial) and registration (from API synthesis to finished product packaging) of a wide range of dosage forms in the EU, US, and Asia.
Learn More
Contact our project managers for more information on quality at UI Pharmaceuticals.