Susan LeePartner at GoodwinSpeaker
Profile
Susan Lee, a partner at Goodwin, advises biologics and drug manufacturers on FDA regulatory and compliance matters that arise in the development and commercialization of new products and indications. She applies her prior business experience in the life sciences industry to provide practical, risk-calibrated solutions. Susan has counseled clients across the spectrum of the industry, from clinical-stage companies to established global players. Susan’s areas of expertise include development pathways; clinical trial compliance; launch preparation, including labeling negotiations, development of promotional claims, and provider and patient engagement strategies; companion diagnostics and digital health tools; and interactions with patients, HCPs, and payors.
Agenda Sessions
Phases of Drug Approval Process
, 9:45amView Session