FDA at SCOPE 2027

Mar 1–4, 2027 Orlando, FL ~5k attendees Website

FDA brings 7 presentations to SCOPE 2027 in Orlando. Its sessions cover the agency's clinical trial innovation efforts and putting quality by design and risk-proportionate oversight into practice. A concrete topic is collecting safety data selectively to make global trials more efficient.

OrganizationSCOPE 2027 Attendance
FDA
Silver Spring, MD
Gov/NGO
US agency that regulates drugs, biologics and medical devices, reviews clinical trial applications and issues trial guidance.
Talk
Mon Mar 1
4:37pm–5:02pm
Panel
Tue Mar 2
9:15am–9:45am
KEYNOTE INTERACTIVE PANEL: From Years to Months: Is Radical Acceleration in Clinical Research Finally Possible?
Plenary · with Duke Clinical Research Institute, Pfizer, Bayer +2 more
Trial design and delivery
Talk
Tue Mar 2
12:20pm–12:45pm
Advancing Global Clinical Trial Efficiency through Selective Safety Data Collection
Trial Design & Protocol Optimization
Talk
Wed Mar 3
9:00am–9:25am
Designing Quality In: Translating ICH E6(R3) into Practice through QbD and Risk-Proportionality
Quality & Monitoring
Talk
Wed Mar 3
9:00am–9:25am
FDA's C3TI: Advancing Innovation in Clinical Trials
Trial Design & Protocol Optimization
Panel
Wed Mar 3
11:40am–12:05pm
Cross-Functional Collaboration and Team Alignment
Advancing Trial Delivery · with GSK, Bristol Myers Squibb, Novartis
Panel
Wed Mar 3
12:05pm–12:30pm
From Requirements to Readiness: Building a Globally-Aligned Regulatory Strategy for Digital Measures for the Next Era of Drug Development
Digital Measures & eClinical Technologies · with AbbVie, Digital Medicine Society (DiMe)

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