ACRO Global Summit
ACRO Global Summit brings together senior regulators and industry leaders from around the world to discuss the evolving regulatory landscape
Universal
Why Do Clinical Trial Startup Delays Still Happen Despite More Technology?
Clinical trial study startup has become increasingly technology-enabled, yet sponsors, contract research organizations (CROs), and research sites still face persistent
The Next Generation of CIRBI, the Technology Powering Advarra’s IRB
A note from Lauri Carlile, Chief Research Services Officer: For more than 40 years, Advarra’s institutional review board (IRB) has
Ensuring Operational Feasibility in Next-Generation Oncology Trials
Our webinar discusses key near-term trends and regulations and investigate persistent challenges frequently throwing even the most efficient teams off track. Advarra and industry representatives will dive deeper into achieving critical milestones across study startup, conduct, and close out that every project manager should optimize.
Data Safety Monitoring Boards (DSMBs) in the Era of AI and Adaptive Clinical Trials
Balancing innovation, statistical rigor, and independent oversight in increasingly complex clinical trials Clinical trials are no longer static. Over the
A More Connected Approach to Clinical Trials: Reducing Friction from Study Design Through Conduct
Clinical trials are complex. That’s expected, given accelerated advancements in science and technology. But when that complexity creates friction in
Gene Therapy Is Seen as the Next Big Biologic in Ophthalmology
Over the last 15 to 20 years, monoclonal antibody-based treatments, such as those targeting vascular endothelial growth factor (anti-VEGF), have
Clinical Oncology Advisory Board
Why we exist Oncology research is moving quickly, and study teams face mounting complexity: novel modalities, new data tools, shifting
Reducing Avoidable Protocol Amendments by Anticipating Operational Pitfalls Hidden in Clinical Trial Design
This white paper examines four KPIs most impacting timelines and budgets and offers strategies for effective communication and risk mitigation.
How Smarter Clinical Trial Study Design Decisions Set Studies Up for Faster Startup and Fewer Amendments
Clinical trial study design forms the foundation of trial success. The decisions teams make at the design stage shape how
Why Research Sites Are Switching to Connected eISF and CTMS
Fueled by automation to remove one of the biggest barriers to adoption Increasingly, research sites are not just asking how
New Paper Makes the Case for AI-Specific Guidance in Research Oversight
AI is becoming a routine part of how research proposals are prepared and reviewed, from drafting applications to supporting administrative