Your Comprehensive Clinical Trial Navigator
Unite Site Staff, Participants, and Study Teams With the Longboat Platform
Ensure compliant and confident execution of the protocol by sites, empower and inform study participants, and efficiently manage and monitor studies within one intuitive platform.
Request a DemoOne Platform. One Team.
All key stakeholders—clinical operations, monitors, site staff, and participants—access one integrated support platform with content tailored to meet their specific needs.
Site Staff
Provide your site staff the tools and resources they need to stay engaged and compliant while focusing on the participant.
Participants
Support participants on their study journey from recruitment through to trial close-out with information and resources they need to be informed, empowered, and to feel appreciated.
Study Staff
Manage global studies by ensuring sites are informed, and engaged, and view real-time data to identify sites that need extra support.
Introducing Secure Document Exchange
Centralize the secure exchange of regulated documents between sponsors, CROs, and sites, significantly streamlining study startup and eliminating historically cumbersome processes across research stakeholders.
All regulatory documents, originating with a sponsor or at a site, can be managed, signed, and securely exchanged to the correct parties for long-term storage into the sponsor’s Electronic Trial Master File (eTMF) and site’s Investigator Site File (eISF) via Advarra eReg.
Enabling study teams to centrally and compliantly,
- Manage documents and document metadata and enable communications within a centralized platform
- Distribute all necessary documents and metadata to sites globally in a consistent and recorded manner
- Request documents required from sites on a global, regional, or single-site basis
- Track and monitor the status of documents and requests
- Route all relevant documents to the appropriate eTMF
Platform Proven to Engage Stakeholders for a Faster and Safer Trial
Site Training Compliance
Enrollment completed 7 months early in a Phase III study
More Longboat Usage
Recruiting vs. non-recruiting sites in a Phase III study
Total Study Enrollment
Achieved by sites that used the pre-screen navigator in a four-study program
Key Platform Features
An integrated toolset ensuring that site staff, participants, and study teams are virtually guided from patient recruitment to study close-out, centrally managed on an advanced, 21 CFR Part 11-compliant platform.
Complete Site Training Solution
Support site staff with study-specific training, including task and event-based training deployment, assessment and certification, and oversight into training completion.
Learn More
Recruitment & Referral Management
Streamline participant recruitment, centralize referral tracking, oversee recruitment metrics and set realistic enrollment goals via Patient Connect within the Longboat platform.
Learn More
Pre-Screening Navigator
Make the pre-screening process easier and faster by allowing sites to complete pre-screening logs on any device, with data being made instantly available to the study team.
Learn More
Participant & Caregiver Engagement
Once enrolled, keep participants and their caregivers informed, engaged, and empowered throughout the study.
Learn More
Study Engagement & Risk Dashboard
Oversee studies with clear dashboards to identify and quickly resolve engagement and compliance issues.
Learn More
Visit Essentials
Ensure site staff and participants remain compliant with clear patient-specific visit walkthroughs, visit reminders, and virtual visits.
Learn more
Medical Animations
In-depth 3D animations of the investigational product’s mechanism of action and study procedures.
Learn More
Feasibility Navigator
Accurately identifies sites with an appropriate patient population based on study eligibility criteria.
Learn more
Integration Ready
Reduce the burden with real-time, two-way data interfaces, including single sign-on, and integration with IRT, EDC, ePRO, and recruitment systems.
Consent Navigator
Increase understanding and ensure informed consent via educational videos for participants.
Learn more
Information and Communication
Ensure targeted communications are prioritized and acknowledged via eSignature.
Learn more
Amendment Rollouts
Seamlessly manage rollouts of protocol amendments and associated training.
Learn more
Additional Longboat Capabilities
A Purpose-Built Clinical Research Cloud Platform
Built upon clinical research best practices, Advarra Cloud is a next-generation platform delivering applications in an easy-to-use, fully managed environment. Learn how the Cloud can help you automate, connect, and expedite processes across the clinical trial lifecycle.
