Luana E. Staiger

Biography

 Luana has 35 years of experience in the regulatory field. Including, preparation and submission of documentation to regulatory authorities; liaise with regulatory authorities on behalf of clients; maintain client files and regulatory correspondence. Assist clients in planning and follow-up for key regulatory meetings (e.g., preIND, end-of-phase 2;preNDA).  Her previous experience includes: 1) Vice President, Regulatory Affairs at ChemGenex Pharmaceuticals, 2) Senior Director, Regulatory Affairs at ICON Clinical Research, 3) Vice President, Regulatory Affairs & QA, Director Regulatory Affairs at Matrix Pharmaceutical, Inc., 4) Associate Director, Regulatory Affairs at Gilead Sciences Inc., 5) Group Manager, Regulatory Affairs at Syntex (USA) Inc.

Research Interest

 Clinical Research