SITE STAFF
Give site staff the tools and resources they need to stay compliant while focusing on patient care.
PATIENTS
Support patients on their study journey from recruitment through to trial close-out.
STUDY TEAMS
Provide study teams with actionable oversight of regional and global site engagement.
ONE PLATFORM
ONE TEAM
Harnessing the latent team energy within clinical trials
Longboat brings site staff, patients, and study teams together on one intuitive platform. All stakeholders have 24/7 access to the information and resources they need to conduct the study using any device type; this creates an environment where protocol compliance is instinctive.
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KEY PLATFORM FEATURES
An integrated toolset designed to ensure that site staff, patients, and study teams are “virtually” guided from patient recruitment to study close-out
Complete Site Training Solution
Engaging training, centrally managed on an advanced, 21 CFR-compliant platform
Patient Recruitment & Referral Management
Raise awareness with engaging, informational websites and centralized referral tracking via Patient Connect
Pre-Screening Navigator
Streamline the pre-screening process by easily generating electronic pre-screening logs via any device
Patient & Caregiver Engagement Platform
Once enrolled, keep patients and caregivers informed, engaged, and empowered throughout the study
STUDY ENGAGEMENT & RISK DASHBOARD
Give study teams the oversight they need to identify and quickly resolve engagement and compliance issues
Visit Essentials
Clear patient-specific visit walkthroughs with automated visit reminders
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Medical Animations
In-depth 3D animations of the investigational product’s mechanism of action
Feasibility Navigator
Accurately identify sites with an appropriate patient population based on study eligibility criteria
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Consent Navigator
Bespoke, engaging videos to educate patients about the trial and ensure truly informed consent
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Integration Ready
Reduce the burden with real-time, two-way data interfaces, including single sign-on and direct integration with IRT, EDC, ePRO, and recruitment systems
Information & Communication
Ensure targeted communications are prioritized and acknowledged via eSignature
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Amendment Rollouts
Seamlessly manage rollouts of protocol amendments and associated training
BRINGING PROTOCOLS TO LIFE
7,175
SITES
24,965
CLINICAL RESEARCH PERSONNEL
55,680
PATIENTS
59
COUNTRIES
73% of clinical investigator-related deficiencies were protocol-related.
More than 80% of physicians use smartphones for professional purposes.
85% of clinical trials fail to retain enough patients.
Simply feeling like you're part of a team of people working on a task makes people more motivated as they take on challenges.
81% of physicians said it is very important for patients to understand what clinical trials are.
20% to 40% of patient non-adherence to the medication regimen and protocol increases the study size and reduces the quality of the study data.
Per patient trials costs can range from $10k to $60k; a 10% improvement in patient adherence can provide substantial savings through a reduced sample size.
LONGBOAT IN THE MEDIA
As seen on Bloomberg and Fox Business Network.
