Overview
- Dr. George Tidmarsh was appointed on July 21 as the permanent director of the FDA’s Center for Drug Evaluation and Research, filling a vacancy that dates back to January.
- Tidmarsh brings decades of biotech leadership to the role, having founded Horizon Pharmaceuticals and served as an adjunct professor of pediatrics at Stanford University.
- He will oversee safety reviews of major therapies, including the abortion pill mifepristone as well as long-established antidepressants and hormone treatments.
- CDER employs nearly 6,000 reviewers but has shed over 3,000 staff through layoffs and buyouts under Kennedy’s leadership, raising concerns about drug approval timelines.
- His industry background offers reassurance to pharmaceutical companies even as experts question the agency’s scientific capacity and its accelerated approval process.