From site care to study data.

Planning a study and wondering how site data reaches your EDC?

A clinical bridge for sponsors, CROs, hospitals and study sites — patient-reported outcomes and imaging records, aligned to the visit and exported to the study's EDC.

Pilot discussions open — scope agreed per study and site.

LIVE2LIFE-CLIN_Link

A clinical bridge for research institutions — brings patient-reported outcomes and clinician imaging records together at the point of care, aligns them to the study visit, and exports structured records to the study's EDC.

Product overview ..

What it does

  • Patient and clinician data in one record — patient-reported outcomes and CT / nodule records meet in the same study record
  • Matched to the study visit — records are aligned to the visit window configured per study; out-of-window items are flagged for site review
  • Structured for the EDC — records are mapped per study and exported to the sponsor's EDC; failed exports are retained and can be replayed
  • Subject IDs only — study records use the study subject ID, not direct identifiers

Who it's for

For the people who run the study and the people who see the patient.

Sponsors & CROs

Structured records arrive aligned to the visit, instead of being reconciled by hand.

Hospitals & study sites

Capture stays inside routine care. Site staff do not run a separate system or a second workflow.

Clinical operations

Pending exports and out-of-window records are visible, so nothing is silently dropped.

How a pilot starts

Three steps, agreed with the study team and the site.

1

Scope

Study, sites, EDC and visit windows are agreed

2

Site readiness

Mapping, pairing and data flow are set up with the site

3

Pilot

Controlled test first, then the site workflow

Talk to us about a study

Tell us the study, the site and the EDC you work with. We will scope the data mapping and visit windows with you.

Or email info@live2life.ltd

LIVE2LIFE-CLIN_Link — a clinical bridge for research institutions.

LIVE2LIFE.LTD supplies only the software tool that implements the specified capabilities. It does not conduct the study, provide regulatory advice, perform validation on the sponsor's behalf, or take custody of study data. Those responsibilities remain with the sponsor and the relevant clinical sites.
LIVE2LIFE-Health_WK · always on