The USCGF has a GMP-compliant Quality System which consists of an organizational structure with policies, procedures, processes, and resources needed to implement a quality management approach for the manufacturing and testing of clinical trial materials, to ensure safety, purity and effectiveness of products.
The USCGF utilizes an electronic document management system, OnBase, for managing controlled procedures and other quality system documentation. Click here to read more about our document system.
Diagram designed by Jade Welch, 2018.
Interim Director, Research Quality and Compliance, Upstate Cell Therapy cGMP Facility