StriQ helps pharma sponsors and CROs start, conduct, and close clinical trials in a single system, automating repetitive manual work across documents and sites, keeping every action traceable, and keeping every decision in expert hands.
Running a trial today means coordinating hundreds of documents, dozens of sites, and many regulatory steps across disconnected platforms and spreadsheets. The result is a workflow that’s slow, error-prone, and difficult to audit.
Status updates and approvals requiring email chains and follow-up calls.
Protocols, consent forms, and site documents living across disconnected systems.
Audit trails that are incomplete, delayed, or scattered across tools.
Intelligent routing and approvals without email chains.
All documents versioned and accessible in one platform.
Complete audit trails logged automatically and always ready.
One connected system, from planning to close-out.
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StriQ replaces fragmented, email- and spreadsheet-driven trial workflows with a single guided platform that spans the full trial lifecycle, like plan, launch, run, and close.
It sits at the center of your clinical trial operations, automating the repetitive work, keeping every action traceable, and giving expert teams the space to focus on decisions rather than paperwork.
Built specifically for the complexity of multi-site, multi-phase trials, StriQ doesn’t just digitize your process. It understands it — flagging risks before they become delays, routing approvals intelligently, and keeping every stakeholder in sync automatically.
Every automated action StriQ takes — from document classification to approval routing — is a proposal, not a final decision. Your team reviews and confirms the actions that matter, so you get the speed of automation with the accountability of expert oversight.
Complete audit trails are logged automatically and stay always ready, so the trial record is audit-ready at close-out rather than reconciled after it.
What StriQ does across every trial you run
StriQ’s AI reads, classifies, and routes trial documents — protocols, ICFs, site agreements, regulatory submissions — automatically extracting key data and flagging inconsistencies before they cause downstream delays.
Configure once, adapt continuously. StriQ’s workflows adjust dynamically as protocols change, sites onboard, or timelines shift, without rebuilding processes from scratch.
Every action, approval, and document version is automatically logged and audit-ready, giving your regulatory and QA teams confidence without the manual reconciliation.
Automated notifications, approval routing, and status updates keep sponsors, CROs, and site teams aligned — without another status call.
StriQ is compliant with 21 CFR Part 11, ALCOA+ and ICH E6, E8, E9, and E10, with CDSCO NDCT 2019 and ICMR ethics guidance embedded by design.
See how StriQ can compress your trial timelines and eliminate manual workflow drag, built for the way sponsors and CROs actually operate.
