Built for the workbetween your systems.

Intelligent infrastructure for clinical research sites: connecting fragmented trial systems, automating workflows and unburdening research staff.

Building for tomorrow's clinical trials.

Let's chat about sites!

Tap a query to clear it0queries and0transcription errors cleared

Trusted by sites working with

Discovery got faster.The evidence didn't.

AI can propose a drug candidate in months. Proving it works still runs through research sites, where coordinators carry data by hand between eSource, EHRs, lab reports and a different EDC for every sponsor.

The same blood pressure gets typed into five builds, five ways. Every value keyed by hand is a query waiting to happen, and every new trial adds more systems for the same people.

~75%
of sites still copy eSource into the EDC by hand
~70%
see transcription errors when they do
~20 min
per visit spent on transcription and cleanup
12–48 h
from visit to data in the sponsor EDC, at best today

So we're rebuilding the layer underneath.

Visit to data in the sponsor EDC

12–48 h today

0 h with Enlace

Transcription error rate

~10% by hand

0% with Enlace

Finally built for research sites.

Collection, verification, entry.None of it has to be manual.

ClinSpark Visit 2, vitals

HR72 bpm

SYSBP 128 mmHg

DIABP82 mmHg

TEMP36.8 °C

RESP16 /min

Systolic BP

128 mmHg

From ClinSpark, Visit 2, 09:41

  • Matches the source
  • In range, 90 to 180 mmHg
  • Inside the visit window
  • No protocol deviation

Awaiting sign-offM. Alvarez, CRCPart 11, 14:02

128 mmHgSystolic BP, signed by M. Alvarez, CRC

  • Medidata RaveVSORRES_SYSBP128
  • Veeva Vaultvs_sysbp_1128
  • Castorsys_bp128.0
  • REDCapvs_sbp_v2128
  • OracleVITALS.SBP128 mmHg

Visit 2 in ClinSpark, kept the way your site keeps it.

Your source

eSourceClinSpark, CRIO, RealTime
EHREpic, Oracle Health, athenahealth
Paper sourceWorksheets, lab reports

The Enlace engine

  1. 1

    Collection

    Read every source the way your site keeps it.

    • Structured and unstructured read-out
    • Digitised source record
  2. 2

    Verification

    Check every value before it moves.

    • Source data verification
    • Data quality and anomalies
    • Protocol amendments
    • Protocol deviations
  3. 3

    Sign-off

    A person on your team approves every value.

    • Coordinator or PI review
    • Part 11 e-signature
  4. 4

    Entry

    Write into each sponsor's EDC.

    • Audit-trailed auto entry
    • Each build in its own format

Each sponsor's EDC build

Medidata RaveVSORRES_SYSBP
Veeva Vaultvs_sysbp_1
Castorsys_bp
REDCapvs_sbp_v2
OracleVITALS.SBP

Conventional eSource would be another tool to learn, integrate and pay for. Enlace works with the source you already keep.

One layer underneath everything.Every trial, every system, one place.

Not a connector for one task: an operating system that moves and reconciles clinical data across your site, with a named person signing off every step.

And the next bottleneck you name. The engine doesn't care which pain it points at.

Inbox

MineEveryoneActiveClosedAll
Assigned
4
In progress
2
Submitted
7
Blocked
1
PacketTrialRecordsExceptionsStatusAssignee
Cohort 3 Day 1 dosingVELA-108263 openBlockedMaria Alvarez
Visit 2, subject 1003VELA-108480 openAssignedMaria Alvarez
Screening, subject 2011ONYX-3011120 openIn progressJames Okafor
Safety labs, subject 0417ARIA-205140 openSubmittedRachel Chen
Query: headache onsetONYX-30110 openAssignedJames Okafor
Visit 1, subject 1001VELA-108480 openClosedMaria Alvarez

The systems that make your day harder.We're here to connect them.

Every sponsor adds another login, another build, another place to type the same value. Enlace connects them into one place.

ClinSparkCRIORealTimeMedidata RaveVeeva VaultCastorREDCapOracle
EpicOracle CernerathenahealthOnCoreClinical ConductorFlorenceAdvarra

Built with research sitesin the US and Europe.

Site networks

One way of moving data across every location, sponsor and EDC, instead of a workaround at each site.

Research practices

Oncology and specialty practices where source lives in the EHR and in lab reports.

Built for compliance from day one. Every site, every time. No shortcuts.

  • 21 CFR Part 11Electronic records and signatures you can defend.
  • ICH E6(R3) GCPData that is attributable, original and accurate.
  • ISO/IEC 27001Security managed end to end, from the first line.

Clinical trials,rebuilt from the site up.

Faster data, fewer queries, more studies. Tell us which eSource and EDCs you run, and we'll show you a transfer on a study like yours.

Let's chat about sites!