Moravek has a philosophy of continuous improvement, which has been enhanced by audits of our facility carried out by our clients’ Quality Assurance departments. This collaboration has resulted in the design and implementation of a comprehensive, GMP-compliant Quality System that has consistently met all essential compliance requirements, both domestic and international.
Moravek is proud to have hosted over one hundred audits by our clients, including some of the world’s leading pharmaceutical companies. Additionally, Moravek’s Drug Manufacturing License was issued by the California Department of Public Health – Food and Drug Branch following an audit of our Quality System.
All audits of our GMP Quality System and facilities have resulted in the determination that Moravek is qualified to prepare GMP APIs for use in early phase clinical trials.