Regulatory Affairs Scientist
Allucent
Bianca Quade, PhD is a rising professional with 10 years of research and industry experience. Dr. Quade has expertise in regulatory medical writing including Health Authority meeting requests/packages, annual reports, designation requests, various eCTD module documents. Also experienced with project management including monitoring product lifecycle management activities, tracking deliverables, risk management, and liaising with internal and external partners.
Sponsored Presentation: Proactivity and best practices in the evolving FDA landscape
Wednesday, October 8, 2025
10:45 AM - 11:10 AM EST