A freelance medical writer with 15 years of experience in the biotechnology industry, Suzanne specializes in regulatory documents that support NDA, IND, and
BLA filings to the FDA. She has composed publications requiring the interpretation of data for a variety of audiences including scientists, medical professionals, and government agencies.
Her project management skills are required for moving projects forward and managing revisions.
Suzanne keeps apprised of new developments in medical writing through professional affiliations and educational workshops.