Linda LaMarreDirector, Medical Writing at Daiichi SankyoSpeaker
Profile
Linda LaMarre is Senior Director of Regulatory Writing at Daiichi Sankyo. With more than 20 years of experience in the pharmaceutical industry, she specializes in regulatory writing, submission strategy, and global regulatory operations. Linda has led regulatory documentation supporting worldwide health authority submissions across multiple therapeutic areas and is a strong advocate for operational excellence, innovation, and process improvement. She is passionate about developing talent, building high-performing teams, and advancing efficient, high-quality regulatory writing practices.
Agenda Sessions
Regulatory Writing to Trial Transparency – Building Consistent Disclosure
, 10:30amView Session
