ModernClinical Trials
Run every clinical trial from a single ecosystem, or find one to join. Trial360 OS unifies study start-up, TMF, sites, regulatory, budgets, and AI for research teams, and helps the public discover active studies worldwide.
Looking for a trial to join? Search active studiesFOR CLINICAL RESEARCH
Clinical research moves the world forward. Too often, the world can't find it.
Trial360 OS exists to close that gap. It gives research teams one system to run trials without friction, and gives the public a plain-language way to find and understand the studies happening around them, anywhere in the world.
Run every trial, at scale.
One workspace for sponsors, CROs, and sites to manage study start-up, TMF, monitoring, queries, safety, and close-out from a single audit-ready workspace. Built for regulated environments, designed for inspection readiness from day one.
See the platformFind the trial.
Search active clinical studies near you or anywhere in the world, explained in plain language.
No medical background needed.
Type a condition and a place. We'll show what's recruiting, who qualifies, and what it involves, in plain English.
Three steps, plain language.
All you need is a condition you're curious about.
Search
Type a condition, medication, or keyword. We translate medical terms into plain language as you go.
Review
See what a study actually involves (visits, procedures, what happens if you join) before you reach out.
Contact
Message the study team directly, or save a study for later. No account or referral required.
Built for people, and researchers.
Everything a listing leaves out, translated into something you can actually use.
Plain-language matches
Medical jargon translated into everyday language, so eligibility criteria actually make sense.
Eligibility snapshot
See age, condition stage, and key requirements at a glance before you read the fine print.
Location & travel
Distance from you, number of sites, and whether remote participation is an option.
Direct contact details
Study contact information up front, so there's no phone tag with a call center.
Downloadable summary
A plain-language summary you can bring to your own doctor to talk it through together.
Ask-a-trial assistant
A simple assistant that answers questions about a specific study, in plain English.
Worth knowing before you search
Trial360 OS surfaces publicly listed studies for information only. It isn't medical advice and doesn't replace your doctor. Eligibility is confirmed by the study team, not by us. If your health situation changes or feels urgent, contact a healthcare provider.
Trial operations shouldn't live in different tools.
Site trackers in one spreadsheet, monitoring visits in another, queries in an inbox. By the time a problem is visible, it's already a delay.
Fragmented systems
Site data, EDC, CTMS, and email live apart, so no one has one current picture of a study.
Manual monitoring
CRAs chase site updates by phone and email instead of reviewing status in one place.
Delayed visibility
Enrollment lags and protocol deviations surface weeks after they happen, not the day they do.
Built for the full arc of a trial, start to close.
One workspace follows a study from feasibility through database lock: the same record, the same team, no re-entry.
Site feasibility
Score and select sites against enrollment history and staffing capacity.
IRB & EC tracking
Track approvals and amendments per site with automatic expiry alerts.
Activation timeline
See every site's path to green-light in one shared timeline.
Enrollment tracking
Live enrollment versus target, by site, country, and cohort.
Monitoring visits
Schedule and log CRA visits with findings tied directly to the site record.
Query & deviation management
Route queries and protocol deviations with owners and due dates.
Data lock readiness
A live checklist of what's blocking database lock, by site.
Site close-out
Standardized close-out packets and sign-off, tracked to completion.
Archival
Every document and decision retained in an audit-ready record.
Visibility that updates the moment a site does.
-
Real-time roll-ups
Enrollment, deviations, and query aging refresh as sites report, with no weekly export.
-
Risk-based monitoring
Sites are flagged automatically when metrics drift outside protocol thresholds.
-
Exportable reporting
Sponsor-ready reports generate directly from live data, not a re-typed summary.
Validated for regulated research, by default.
Every record change is signed, timestamped, and retained, so it holds up under sponsor and regulatory audit.
- QC approved · Site 104 · Delegation log v2M. Okafor, QC reviewer · reason: complete
- Signed · Protocol amendment 3Dr. L. Chen, Principal Investigator · meaning: approval
- Version superseded · Informed consent v4 → v5A. Ruiz, Study coordinator
- Filed to TMF · 05.02.01 IRB approvalS. Patel, CRA
“We closed our last database lock nine days ahead of plan. That's never happened before Trial360.”VP, Clinical Operations · mid-size CRO
Ready to run trials without the spreadsheets?
See Trial360 OS on a live study workspace, walked through by our team.