Tryal Accelerator
Faster. Smarter. Better.
Tryal Accelerator speeds clinical trial startup by generating high-quality documents from the study materials you already have, using your template or ours. Whether it’s a protocol, meeting transcript, or prior draft, Accelerator pulls from your full study knowledge base and cites every source for clarity and confidence. The result is faster, more consistent documents that get your study to first patient in, faster.
Document Generation,
Done Intelligently
Produce ICFs, all of your clinical plans, site training materials, and more using content from across your study materials, not just the protocol. Everything is cited for transparency and traceability.
Template-Driven,
Audience-Aware Content
Reusable templates with built-in prompts ensure consistency and regulatory alignment. Set the audience for each document to guide tone and structure - whether writing for sites, participants, or internal teams.
Built for Compliance,
Proven Through Validation
Accelerator complies with 21 CFR Part 11, offers role-based access controls, and ensures full traceability of generated content. Validated by Tryal and aligned with GxP principles, it can be confidently integrated into your organization’s CSV framework.
AI That Works With You
You stay in control. Limit generation to your knowledge base, or include broader information sources, surface only what matters, and get clear references every time. No guesswork. Just fast, reliable content built on what you trust.
Your Workflow, Accelerated
Tryal Accelerator fits into how your team already works. Whether you’re revising a draft or starting from scratch, it makes the process faster, easier, and more consistent.
Tryal eCOA
Deep Expertise. Faster Start-Up.
Better Data.
Tryal eCOA makes data collection simple and keeps participants engaged. With decades of experience building smart, easy-to-use eClinical solutions, our eCOA combines all the essential tools to support today’s global clinical trials—without unnecessary add-ons that complicate workflows. Everything you need, nothing you don’t, for faster, streamlined studies with dependable results.
Built by eCOA pioneers, Tryal seamlessly combines efficiency with data integrity and regulatory discipline.
Comprehensive eCOA Data Capture
Collect critical data–either online or offline– with support for ePRO (patient-reported), ClinRO (clinician-reported), ObsRO (observer-reported), and PerfRO (performance-based outcomes) across iOS, Android, and web platforms. Our open API ensures you can get any eCOA data where you need it, when you need it. Flexible design adapts seamlessly to the unique requirements of any clinical study.
Rapid Study Setup
Accelerate timelines with our library of pre-built, validated instruments, visual configuration tools and rapid prototyping. Tryal’s flexible eCOA solution and experienced service team can adapt to your trial’s requirements—reducing setup time while ensuring clinical precision.
Participant-First Engagement
Keep participants engaged with intuitive mobile apps, televisit capability, and customizable reminders, alerts and alarms. With six direct communication options, you can improve compliance, reduce dropouts, and enhance data quality.
More Reliable Source Data
Optimize your trials with smart scheduling and real-time data validation. Our advanced scheduling module keeps patients on track and ensures visits run smoothly. At the same time, real-time data validation catches errors upfront, so you get clean, reliable results faster and reduce time spent correcting mistakes.
Trusted Support for Global Trials
Partner with a team that delivers on its promises. From eCOA licensing and consulting to translations, localizations, device provisioning, and native language call support worldwide, our experienced team is here to help. With clear communication at every step, you can rely on us to navigate challenges and ensure your trials succeed—wherever they take place.
Simplify data collection with Tryal eCOA.
Tryal eConsent
Consent Made Simple, Powerful, and Personal.
Tryal eConsent breaks down barriers between research and participants. We make enrolling in a study straightforward, understandable, and empowering—for everyone involved.
Tryal eConsent turns consent from a hurdle into a handshake—connecting researchers and participants with unprecedented ease and clarity.
Anytime, Anywhere Access
Allow participants to sign consent from their phone, tablet, or computer – no paperwork, no delays.
Lightning-Fast Setup
Go from study protocol to active recruitment in record time.
Crystal-Clear Understanding
Interactive guides, multimedia tools, and localized content help participants truly understand what the study means for them.
Global Compliance
Meet international regulatory standards with e-signatures and 21 CFR Part 11-compliant options for secure, worldwide recruitment.
Seamless Re-Consent
Empower participants to quickly review and provide consent to updated trial information at their convenience, helping them feel more informed and engaged throughout the process.
Real-Time Visibility
Track every consent interaction instantly with complete transparency and security.
Simplify your consent process with Tryal eConsent.
Configurable Workflows Standards
Enforce clear, consistent standards for home visits, globally.
Real-Time, Validated
Home Health Data
Validate information at the point of care with intelligent e-source data capture.
Provider Screening
and Credential Verification
Streamline service provider credential verification and approval with our seamless, standardized workflow for uploading and validating licenses and certifications.
Smart Staffing
Easily schedule primary, backup, and emergency providers to ensure uninterrupted coverage for all remote visits.
Take control of remote studies with Tryal Home Health.
Tryal Video
Anonymization
Protect Privacy, Preserve Data Integrity.
Tryal Video Anonymization helps safeguard patient privacy in clinical trial videos, reducing risks while maintaining the integrity of critical research data. Powered by Tryal Accelerator, our technology streamlines the anonymization process, removing all personally identifiable information (PII) without compromising the quality of the clinical insights.
Privacy Protection
Advanced algorithms blur faces and redact audio, eliminating PII to keep participant identities confidential.
Regulatory Compliance
Fully validated processes meet standards such as HIPAA and 21 CFR Part 11.
Re-identification Prevention
Anonymized data is irreversible, with rigorous safeguards to prevent any attempts at re-identification.
Participant Trust
Anonymization builds confidence in clinical trial processes, encouraging participation while fostering research integrity.
Protect patient privacy with Tryal Video Anonymization.