Our Approach
Bringing you the insights and efficiency that study design, site identification and feasibility, activation, and enrollment demands.
Intelligent
Turn industry-leading intelligence and operational data into smarter study design, better site selection, and earlier risk detection.
Automated
Automate critical workflows through deep integrations with the industry’s most site-native systems to improve accuracy and accelerate activation.
Already Adopted
Built with and for sites, our solutions fit naturally into 35,000+ site workflows to drive real adoption and reduce operational burden.
Transparent
The only purpose-built space where sponsors, CROs, and sites get shared, real-time visibility into study progress to keep studies moving.
Study Collaboration solutions
Advarra’s Study Collaboration solutions help you design operationally feasible studies, partner with the right sites, and execute efficiently together.
Optimize protocols with insights from the industry’s richest trial operations dataset, including digitized protocols, study documents, and operational data from Advarra’s IRB to prevent avoidable amendments and downstream delays.
Identify sites using the most up-to-date performance and compliance data from IRB insights, then accelerate site qualification through streamlined feasibility assessments.
Activate sites quickly via guided workflows that provide shared visibility and automate progress towards site readiness to start studies faster.
Collaborate with sites more efficiently through connected document exchange and AI-powered study training that prevents deviations and reduces disconnected communication.
Enable sites to prioritize your referrals with direct integration to their CTMS and gain real-time visibility into recruitment progress to convert every potential participant quickly.
Integrated with Your Core Systems (CTMS, eTMF, etc.)
Better collaboration without extra work
Study teams like you rely on systems like eTMF and CTMS to manage portfolios, track milestones, and ensure compliance, but these systems weren’t built for real-time, collaboration with sites. Our solutions seamlessly integrate with your existing workflows, automatically delivering documents, updates, and startup materials into your systems of record while providing a shared workspace for you and your sites to work together.
Integrated with Critical Systems Sites Use Every Day
Ensure your study is prioritized
Sites depend on their own CTMS, eReg, and other operational systems to manage finances, staffing, regulatory compliance, and more across their full research portfolio. We plug directly into that ecosystem, so your study reaches the teams who will act on it in the tools they already trust, while maintaining shared visibility for sponsor and CRO study items into study-specific activities.
Connecting 225,000 users across 89 countries and counting for more efficient, less burdensome trials.
1 out of 3 identified as avoidable in a Phase III oncology study design
In a phase II multi-cohort study, sponsors using Advarra eliminated 300 emails per day previously needed to exchange documents with sites
In a phase III study across 28 sites, sites using Advarra achieved 98% training compliance over 648 site staff across four years
In a phase III study across 28 sites, the sponsor achieved total enrollment targets seven months earlier than planned
How our user community is tackling today’s greatest industry challenges
Improving Clinical Tech Adoption: Site-Centric Approaches
Advarra research partners explore how a site-centric approach can reduce friction in clinical technology adoption by addressing real-world site challenges and aligning tools with how sites actually work.
Site-Centric Strategies to Fast Track Study Startup
Advarra research partners explore site-centric strategies that improve collaboration, reduce redundancy, and accelerate study startup by better aligning people, processes, and technology.
Building More Feasible Oncology Trials: Data Informed Study Design
Advarra research partners explore how data-informed and AI-enabled protocol design can reduce complexity, improve feasibility, and enhance execution in oncology clinical trials.
Ready to learn more?
Request a demo to see how you can optimize your operations from concept through conduct