Win More Trials. Grow Your Site.
The directory where research sites get discovered — by sponsors, CROs, and the AI tools they use. Structured profiles, AI-powered trial matching, and a full clinical research platform.
How It Works
From signup to your next trial in three simple steps.
1
Create Your Profile
Build an AI-optimized profile with your PI, therapeutic areas, equipment, and patient population — discoverable by search engines and AI tools.
2
Get Matched
Our AI curates a personalized feed of trials from sponsors and CROs that fit your site.
3
Win Trials
Prove feasibility with real patient data, connect with sponsors, and land contracts.
1
Create Your Profile
Build an AI-optimized profile with your PI, therapeutic areas, equipment, and patient population — discoverable by search engines and AI tools.
2
Get Matched
Our AI curates a personalized feed of trials from sponsors and CROs that fit your site.
3
Win Trials
Prove feasibility with real patient data, connect with sponsors, and land contracts.
Everything Your Site Needs
From getting discovered to managing trials, all in one platform.
Site Directory
List your site in an AI-optimized directory. Get discovered by sponsors, CROs, and the AI tools they rely on.
Regulatory AI
Ask regulatory questions, search cited guidance, and keep your site compliant and secure.
EHR & Patient Feasibility
Connect your EHR or patient database to prove your patient population and feasibility with real data.
Community & Chatrooms
Join a network of research professionals. Share insights, find collaborators, and stay connected.
Showcase Your Site
Build a comprehensive profile that helps sponsors find exactly what they need.
Lead PI & Credentials
Therapeutic Areas
Equipment & Facilities
Past Studies & Experience
Patient Population
Location & Catchment Area
The Site Directory Built for AI
Every profile is structured for AI crawlers and search engines. Sponsors and CROs find you whether they're browsing Google, asking ChatGPT, or querying Perplexity.
Regulatory AI Assistant
Ask questions about FDA regulations, warning letters, and ICH guidelines. Get cited answers from real regulatory documents -- not hallucinations. Powered by 3,000+ FDA warning letters, 380+ CFR sections, and ICH guideline PDFs.
Security & Privacy
Built for sensitive clinical research data
Tundra keeps user-submitted data private. Regulatory AI uploads, prompts, proprietary documents, PHI, and AI outputs are not used for model training, telemetry, or analytics.
HIPAA safeguards
BAAs are available for organizations submitting PHI to Tundra.
Private by design
User-submitted documents, prompts, and outputs stay private.
Not used for training
Customer data is not used to train AI models or shared for analytics.
The Full Platform
Beyond trial matching, manage every aspect of clinical research in one place.
AI Patient Screening
Automated eligibility evaluation from EHR data with AI and voice agent follow-up.
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Document Store
Version-controlled documents with e-signatures and full audit trails.
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Regulatory AI
AI-powered regulatory research assistant with cited answers from FDA, CFR, and ICH sources.
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Identity Verification
KYC/AML verification and fraud detection for participant onboarding.
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Participant Payments
Direct-to-bank compensation via ACH, RTP, and FedNow.
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Don't Let the Next Trial Pass You By
Research sites on Tundra Space get found by sponsors, CROs, and AI tools — match to trials faster, prove feasibility with real data, and never miss an opportunity.
Questions? Contact us at research@tundraspace.com