Connect with our team at SCOPE Summit 2026
Connect with our team at SCOPE Summit 2026
By Sofía Sánchez González
Clinical trials are the engine of medical progress, driving new treatments, improving outcomes, and advancing scientific knowledge. Their success depends on collaboration, innovation, and strategic execution at every step.
That is exactly why SCOPE has become a must-attend event for the clinical research ecosystem.
SCOPE Summit returns February 2–5, 2026 in Orlando
Now in its 17th year, SCOPE Summit returns February 2 to 5, 2026, at Rosen Shingle Creek in Orlando, Florida, bringing together the full clinical research community for four high-impact days of discussion, strategy, and networking.
Why SCOPE continues to set the pace for clinical trial innovation
SCOPE 2025 convened 4,500+ attendees, 630 speakers, and 300 exhibitors, with 60% in key decision-making roles, reinforcing its position as a premier event for clinical trial innovation.
What to expect in the 2026 program
The 2026 agenda expands coverage of the topics clinical research leaders are prioritizing right now, including development planning, protocol optimization, patient-centric trial design, site engagement and recruitment, generative AI, small biopharma strategies, RBQM, supply and clintech investment.
Each track is designed to support better trial planning, stronger operations, and faster innovation across the clinical trial lifecycle.
Let’s connect at SCOPE Summit 2026
SCOPE Summit welcomes senior executives from pharma, biotech, CROs, research sites, technology, investment, and patient advocacy organizations, representing 1,200+ companies across 30 countries.
If you are attending Scope Summit 2026, we would love to connect. Reach out to schedule a time with our team onsite.
About Narrativa
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For companies in the life sciences industry, Narrativa® Navigator provides secure and specialized AI-powered automation features. It includes complementary user-friendly tools such as Clinical Atlas, Narrative Pathway, R-Developer for TLFs, and Redaction Scout, which operate cohesively to transform clinical data into submission-ready regulatory documents. From database to delivery, pharmaceutical sponsors, biotech firms, and contract research organizations (CROs) rely on Narrativa® to streamline workflows, decrease costs, and reduce time-to-market across the clinical lifecycle and, more broadly, throughout their entire businesses.
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