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.
Quality Assurance (QA) Services for Clinical Trials in the EU
The University of Iowa Pharmaceuticals (UIP) offers comprehensive Quality Assurance (QA) services, including access to a Qualified Person (QP) for sponsors seeking QP release for their products in clinical trials across the European Union. Our QP certification ensures compliance with EU regulations, providing peace of mind for your clinical trial needs.
At UIP, we bring extensive experience in Chemistry, Manufacturing, and Controls (CMC) activities, covering the entire spectrum from development to commercial manufacturing and registration. Our expertise spans API synthesis, finished product packaging, and a wide range of dosage forms. We serve clients in the EU, US, and Asia, ensuring global compliance and quality.
Partner with UIP for your QA needs and benefit from our proven track record in delivering high-quality pharmaceutical solutions.
Learn More
Contact our project managers for more information on quality at UI Pharmaceuticals.