Richard Edmunds

Contact Details


Senior-level regulatory affairs professional and regulatory project manager.
15+ years of broad regulatory experience in regulatory affairs, CMC, clinical, and manufacturing, in US, EU and international markets.
Expert regulatory consultant responsible for establishing and managing long-term, large-scale regulatory projects and teams, from clinical development to new product filings and post-approval activities for pharmaceutical, biologics and consumer health products.

Strengths: Regulatory Strategy, New product registration, Regulatory Authority interactions and negotiations, CTD document authoring and review, IND and Clinical Trial Applications, Labelling, Lifecycle management and Global regulatory Intelligence.

Job History

G&L Scientific
Vice President Regulatory Affairs
September 2017 - present