Just shipped
Remote eligibility, without the privacy tradeoff
Participants can screen from home. Criteria that need a coordinator stay pending until staff verify them, while answers and identity remain on the participant side of the privacy boundary.
Study supplies that come to you
Track a study kit, report a damaged delivery, and confirm receipt with the kit code from the app. Research teams get the accountability trail they need through return or final disposition.
Risk-based monitoring in one view
Write the monitoring plan, track deviations, and review six live risk indicators without crossing the blinding or identity boundaries. Thin data stays “not enough data,” never a false alarm.
A real voice before the protocol is final
Review a short, plain-language protocol digest and rate what feels workable. Feedback is pseudonymous, optional, and hidden from research teams until enough people respond.
From startup checks to a verifiable archive
Launch readiness, protocol versions, trial-registration clocks, milestones, reconciliation, audit inventory, and closeout now form one governed path from draft study to hash-stamped archive.
An inspection package that knows what it contains
The unified audit export carries a machine-checked inventory across every study-scoped audit domain, with de-identified participant events and blinding-safe unblinding records.
Also recently
Regulatory activation & IRB oversight
No enrollment or randomization without a current IRB approval bound to the exact protocol and consent versions it covers. Generate submission packets from structured data, and track amendments and reportable events in one regulatory hub.
Randomization & blinding
Permuted-block, minimization, uploaded-list, or simple randomization for everyday RCTs and crossovers, with open, single, and double-blind modes, a code-versus-arm firewall, and an audited emergency unblind.
A baseline that banks itself
Wearable data can start collecting before you enroll, and recent coverage waives the baseline wait when a study begins. A configurable baseline window and wearable sync-health surface gaps early.
eConsent, made humane
Accessible, resumable informed consent with gentle comprehension checks, a 21 CFR Part 11 e-signature, and a countersigned PDF receipt. Consent that respects a hard day and can be re-read anytime.
Adaptive platform trials
A perpetual, multi-arm protocol with deterministic randomization, response-adaptive allocation inside preset guardrails, factorial domains, and a blinding firewall that keeps interim looks away from the people who shouldn’t see them.
Electronic data capture + CDISC export
A versioned, audited dataset with an edit-check engine and query workflow, MedDRA/WHODrug coding, soft and hard database lock with audited unlock, and one-click CDISC SDTM + define.xml export.
Pacing & readiness
A within-person heart-rate ceiling, time-over-threshold, an orthostatic-aware POTS split, and a morning readiness read from resting HR and HRV — framed as a pattern, never a prediction. Quiet by default.
Patient-led self-trials
Guided single-case (n-of-1) studies with on-device single-case experimental design and segmented-regression analytics, a primary endpoint you choose, and an honesty layer that won’t let a hopeful trend pose as proof.
Study results & history
A calm, within-person Green / Yellow / Red read of your own measures — never red on missing data — plus a unified history of every study and self-trial you’ve run.
Objective PEM capture
Post-exertional malaise detected from ordinary participation — check-ins plus wearable data — against a versioned, patient-anchored definition, with a tap-only enrichment flow.
Gentle investigator nudges
A coordinator can queue a one-way, templated check-in that arrives as a considerate local notification — rate-limited, never stacking, and silent when someone is unwell.
Adverse-event safety & escalation
A reporter-not-actor model so the person who notices a safety concern isn’t forced to act, with instant routing and a privacy wall between identity and clinical data.