Study Startup (SSU) Solution for Sponsors and CROs
Accelerate Study Startup Across Stakeholders
The only site-sponsor collaboration solution giving you immediate visibility to help you hit every study startup milestone on time, including ethics review, so you can start enrolling sooner.
1NEW1 Advarra integrates study startup and IRB technologies, enabling unprecedented visibility into clinical trial site activation.
True Site-sponsor Collaboration, Not Another Investigator Portal
Your sites are our trusted partners. Around 50,000 site staff log into Advarra applications every month. Meet sites where they are, in a solution that fits their existing workflows. Expand visibility to critical milestones, including institutional review board (IRB), while giving sites choice.
Erin Williams, SVP of Study Startup with Velocity Clinical Research speaks to leveraging Advarra services and technology to improve startup timelines and collaboration with sponsors.
The Future of Study Startup
Give sites flexibility, while ensuring total visibility for study teams like yours, all in one study collaboration solution.
Site Feasibility
Quickly gather information about potential site partners with a workflow tool to combine multiple site lists, route for review/approval, distribute feasibility surveys, and track site status.
Single Sign-on (SSO) Hub
Enable site teams to use their own organization’s login, improving security and reducing time spent on technology access and setup throughout activation and conduct.
Guided Activation
Track progress on study startup milestones with visibility into site selection, ethics approvals, finalized contracts, greenlight documents, and more. Ensure alignment and progression across each critical path step.
Document Exchange
Accelerate study startup via end-to-end integration between the electronic trial master file (eTMF) and sites’ electronic investigator site file (eISF). Including automated, seamless exchange of research documents between sites, sponsors, contract research organizations (CROs), and Advarra IRB, without the need to manually download and reupload documents between systems.
Study Training
Support site staff with engaging, animated, study-specific training content including task- and event-based training deployment, visit guides, assessment and certification, and oversight into training completion. Ensuring site staff are ready to enroll and execute your study.
Trusted Study Startup Solution, Proven Results
Connecting 225,000 users across 89 countries and counting.
In a phase II multi-cohort study, sponsors using Advarra SSU eliminated 300 emails per day previously needed to exchange documents with sites
In a phase III study across 28 sites, the sponsor achieved total enrollment seven months earlier than targeted
In a phase III study across 28 sites, sites using Advarra SSU achieved 98% training compliance over 648 site staff across four years
Start Clinical Trial Enrollment Sooner
