Rethinking Oncology Trial Design: Turning Insights from Data and Experience into More Feasible Studies
Estimated reading time: 4 minutes Oncology research continues to push scientific boundaries, from biomarker-driven...
FEATURED E-BOOK
Making Good Clinical Practice More Understandable
This eBook dives into GCP’s role in the clinical research ecosystem and how it protects participant rights, safety, and confidentiality.
Preparing for Elsa: What Sponsors, Sites, and CROs Need to Know About the FDA’s New AI Era
Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments....
Simplifying Oversight and Managing Regulatory Complexity in Multi-Site Clinical Trials
Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments....
Q&A with Advarra’s Client Experience Team Lead Jennifer DeZurik
Estimated reading time: 3 minutes Client Experience Team Lead Jennifer DeZurik brings both professional...
How to Select a Clinical Trial Management System
Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments....
Integrating AI to Balance Scientific Rigor and Real-World Feasibility in Clinical Trial Study Design
Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments....
How Sponsors Can Use Adaptive and Platform Trial Models to Reduce Amendments and Accelerate Study Start-Up
Traditional clinical trial designs often delay progress due to rigid protocols and frequent amendments....
Q&A with Advarra’s Client Experience Partner Brian Boggs
Estimated reading time: 3 minutes As a member of Advarra’s client experience team, Brian...
Enabling Oncology Site Success: Tackling the Barriers That Slow Cancer Research
Estimated reading time: 8 minutes Oncology clinical trials are becoming increasingly complex, placing new...
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