Clinical trial project management with compliance built in
Tasks, milestones, sites and participants in one workspace, kept up to date by the people doing the work.
Every change is recorded with who made it, when and the previous value.
- 21 CFR Part 11 aligned
- GxP validation documentation
- GDPR compliant
Most trial tracking runs on tools built for something else
Nobody can say where the trial stands
Your trial lives across five spreadsheets, three shared drives and someone's personal tracker. No single version is complete. Every status update starts with an hour of reconciling.
When leadership asks "where do we stand?", the honest answer is "give me an hour."
An audit trail you can't produce
Generic tools record content without context. There is no audit trail linking a task change to the person who made it, when or why.
When an inspector asks how you maintained oversight, the answer is a folder of screenshots and a hope that version control held.
Updating trackers eats the week
Your project managers spend more time maintaining trackers than moving trials forward: updating milestones, cross-referencing data, chasing confirmations.
Everything your study team tracks, linked and audit-trailed in one place
Studies, sites, vendors and participants come built in, so there's nothing to set up before your team starts.
We'll migrate your spreadsheets to TrialTrack for free
Already in spreadsheets? Sign up for any paid plan, send us your files and we'll import everything into TrialTrack at no extra cost.
See pricingWhat changes for each role on the study team
Clinical Project Manager
"I spend more time updating trackers than actually managing the trial."
Tasks, milestones and who owns what sit in one workspace, updated by the people doing the work, so you stop maintaining a tracker on the side.
Head of Clinical Operations
"I need to see across all my studies without chasing people for updates."
Filter your Gantt chart by study, build custom tables to surface exactly the data you need and export it when stakeholders ask.
Quality Assurance
"We need to demonstrate oversight, not reconstruct it the week before an inspection."
Every task, status change and assignment is audit-trailed automatically.
Role-based access and full traceability mean inspection evidence accumulates as teams work.
Validation documentation and human-readable release notes are available directly inside the application.
Study Director / Sponsor Leadership
"I ask for a status update and get a different answer depending on who I ask."
Data is entered once, by the person doing the work, so the status you see is the status.
CRO Programme Lead
"Every sponsor wants oversight reported differently, and we rebuild our tracker each time."
Set up each sponsor's study in the same structure, then give each sponsor the custom table or export they ask for.
Clinical structure and compliance, without a CTMS budget
Purpose-built for clinical trials
TrialTrack was designed from day one around studies, vendors, sites and participants, the things clinical teams manage every day.
Generic project tools make you build that structure yourself. In TrialTrack it's there when you sign up.
Compliance on every plan, including Free
An audit trail aligned with 21 CFR Part 11 on every object, role-based access control, and GxP validation documentation with plain-language release notes inside the app.
None of it sits behind a premium tier or an add-on module.
Between spreadsheets and an enterprise CTMS
Spreadsheets work well until several people and studies depend on them. An enterprise CTMS takes six months and six figures to implement, and you will use half the features.
TrialTrack gives you the structure, traceability and compliance your trials need without the procurement cycle.
Running this afternoon
Sign up and invite your team. There's nothing to install or configure, and on a paid plan we'll migrate your existing data for you.
Set up your first study today
Free for up to 3 users, with no credit card and no sales call. You can be up and running in under an hour.