LuAnne Farr
Director of Operations
Ms. Farr brings 21+ years of experience in the biotech industry with a unique blend of medical device and drug development backgrounds. She has extensive experience in managing people and leading multi-functional project teams in all aspects of the FDA-regulated medical device product development cycle. LuAnne has specific expertise in program management, in-vitro diagnostic assay design, product development, design control processes, quality systems, ISO/GMP environments, regulatory submission documentation (510K, PMA, CE Mark) and Phase 1-4 clinical drug trial management.
