Continuous quality oversight

Compliance control for the way clinical research actually moves.

Cairnsplice — Continuous compliance control for clinical research teams

Cairnsplice continuously connects protocol milestones, regulatory deadlines, data integrity signals, and deviations—so distributed study teams can see risk, assign the next action, and keep an audit-ready record.

For sponsors, CROs, research sites, and study teams.

Study oversight / active view

CS-042 · Phase III
Live signals

Current quality posture

Stable

Protocol milestone

Visit window alignment

On track

12 sites

Regulatory deadline

IRB continuing review

Due in 6 days

Owner assigned

Data integrity

Source-to-EDC variance

Investigate

3 findings

Last reviewed 09:42 UTCAll actions assigned

The Cairnsplice control loop

Turn scattered study activity into a visible line of accountability.

Clinical operations rarely break in one dramatic moment. Cairnsplice helps teams catch the small inconsistencies early, before they become a finding, a delay, or a last-minute evidence hunt.

01

Watch

Collect the signals that shape study risk.

02

Connect

Join milestones, deadlines, deviations, and owners.

03

Act

Route the next corrective action before drift compounds.

04

Prove

Keep the decision trail ready for the next review.

Built for oversight

More signal. Less compliance archaeology.

Connect the systems and practices your team already relies on—eTMF, EDC, QMS, and human judgment—then give every decision a place to land.

01

Risk-based quality management, made operational

02

Centralized oversight across sponsors, CROs, and sites

03

Audit-ready reporting without the end-of-study scramble

Start with the pressure point

See what continuous oversight could remove from your next study review.

Tell us where your team is losing signal today. We’ll show you how Cairnsplice can connect the work, route the action, and preserve the evidence.

Request a demo or pilot

cairnsplice-l6rnak@polsia.app

Grounded in 11+ years of healthcare and clinical research informatics experience.

ICH-GCP · ICH E6(R3) · 21 CFR Part 11