Bringing Stem Cell Cures to the Clinic: UC Davis GMP Facility

The FDA requires the use of a Good Manufacturing Practice (GMP) facility for taking stem cell-based therapies into clinical trials. This GMP facility is a clean-room laboratory that ensures the therapeutic products will be safe and contamination-free for patients. In Spring 2008, CIRM gave $272 million for the construction of twelve stem cell research facilities in California. The University of California, Davis was one of the recipients of this Major Facilities grant. Their $20 million ...
Tags: cirm california institute regenerative medicine stem cell research embryonic university davis gmp good manufacturing practice proposition 71 therapy nolta gerhard


















