Galen Neher has extensive experience in the pharmaceutical and quality assurance sectors, primarily with Syntex since 1977, where the role of Alumni has been held. Between 2001 and 2009, Galen served as an Independent Consultant, focusing on investigator site audits, CRO audits, and SOP management, as well as conducting GCP seminars and assisting with FDA inspections. Prior experience includes the position of Associate Director of GLP and GCP QA at Syntex/Roche from 1977 to 1986, overseeing a team responsible for GLP and GCP audits and FDA inspections in the US and UK. Galen Neher earned a PhD in Experimental Pathology from Oregon Health & Science University from 1964 to 1969.
Sign up to view 0 direct reports
Get started