IRB Reportable Events Checklist
Determining whether an event requires prompt institutional review board (IRB) reporting is an important part of protecting research participants, supporting effective
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What Is the Difference Between an SAE, AE, and UADE in Clinical Trials?
Adverse events (AEs) are untoward medical occurrences in participants receiving a study intervention, regardless of whether they’re related to the study. Serious adverse
Meeting Sites Where They Are: A Connected, Intelligence-Powered Operating Model
Meeting Sites Where They Are: A Connected, Intelligence-Powered Operating Model This on-demand webinar, presented by ICON, Advarra, and Fierce Pharma,
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
Rethinking Site Training: A Risk-based Model of Reuse and Reciprocity
Clinical trial site training is supposed to do one essential thing: Prepare site staff to execute a clinical trial safely,
21 CFR Part 11 and Good Clinical Practice Requirements Explained
Clinical research increasingly depends on electronic systems to support core trial documentation, data handling, and regulated workflows. That shift has
London Innovation Summit: Let your network know you’ll be there!
Heading to the Advarra Innovation Summit in London? Share the news and encourage your peers and partners to join you!
When Do Clinical Trials of mRNA Products Fall Under IBC Review
Discover how AI and analytics are transforming clinical trial operations, from study startup to accrual workflows, in this insightful whitepaper.
Launching Advarra Voice to the Site Community
In this webinar, leaders from cancer centers and biopharma companies will discuss the operational and institutional hurdles sites face and what can be done to address them. The panel will explore practical strategies to reduce burden, improve collaboration, and create a better experience for research staff and patients alike.
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
Leveraging Advarra’s Strategic Enablement Services to Improve Research Site Efficiency
In this webinar, leaders from cancer centers and biopharma companies will discuss the operational and institutional hurdles sites face and what can be done to address them. The panel will explore practical strategies to reduce burden, improve collaboration, and create a better experience for research staff and patients alike.
Beginner’s Guide to an Electronic Data Capture (EDC) Systems
This post walks you through the basics of an electronic data capture system, providing a high-level overview of benefits and common functionality.