Digital Source Records

Capture at the source. Eliminate transcription forever.

Digitize source documentation at the point of care. eSource data flows directly into your EDC — no transcription, no delays, no errors.

Join 50+ forward-thinking clinical teams

Patient Visits
Source Forms
Query Log
JR
Patient 101-004
Visit 3 · Screening
Complete
MK
Patient 101-007
Visit 5 · Treatment
In Progress
AL
Patient 102-001
Visit 2 · Baseline
Pending
TS
Patient 102-003
Visit 7 · Follow-up
Complete
Vital Signs — Visit 3
Systolic BP
122 mmHg
Diastolic BP
78 mmHg
Heart Rate
72 bpm
Temperature
36.8 °C
Weight
74.2 kg
SpO₂
98%
Synced to EDC

Powering trials across leading research organizations

Lilly
Sanofi
AstraZeneca
Biogen
Zurabio
Olema Oncology
Visit 3 — Screening Assessment
6 of 8 sections complete
Demographics
Vital Signs
Medical History
Concomitant Medications
Lab Results
Physical Examination
ECG Assessment
Investigator Signature
eSource Capture

Capture source data digitally — right at the point of care

Purpose-built source forms replace paper worksheets. Coordinators enter vitals, assessments, and observations directly into Clincove during the patient visit. Data is structured, timestamped, and audit-trailed from the moment it's captured.

  • Protocol-driven visit checklists
  • Configurable source form templates
  • Real-time validation & range checks
  • 21 CFR Part 11 compliant timestamps
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EDC Integration

Source data flows directly into your EDC

No double data entry. No transcription errors. Source fields are automatically mapped to EDC CRF fields, so data entered at the site populates the sponsor's database in real time. Every value is traceable back to the original source record.

Zero transcription errors
Automatic field-level mapping
Full source-to-CRF traceability
Eliminates SDV bottlenecks
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Source Record
Systolic BP 122
Heart Rate 72
Temperature 36.8
Weight 74.2
Auto-mapped
EDC CRF
VS_SYSBP 122
VS_HR 72
VS_TEMP 36.8
VS_WEIGHT 74.2
Source Record
Systolic BP 122 mmHg
Heart Rate 72 bpm
Temperature 36.8 °C
Weight 74.2 kg
SDV
EDC CRF
VS_SYSBP 122 mmHg Match
VS_HR 72 bpm Match
VS_TEMP 38.6 °C Mismatch
VS_WEIGHT 74.2 kg Match
Source Verification

Remote SDV, built right in

Monitors verify source data against CRF entries without visiting the site. Side-by-side source and EDC views let CRAs complete SDV remotely, flag discrepancies, and resolve queries — all within a single platform.

Side-by-side source vs. CRF view
Remote SDV with full audit trail
Inline query creation & resolution
Reduces monitoring visit costs by 60%
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Visit Management

Protocol-driven visits, enforced automatically

Protocol-defined visit windows are enforced automatically. Coordinators see upcoming visits, overdue assessments, and deviation alerts at a glance — keeping your trial on track without manual oversight.

Protocol visit window enforcement
Overdue visit alerts
Window deviation tracking
Dynamic visit schedule view
Have Questions?
Visit Schedule — Study 2024-001
Visit 1 — Screening
Feb 12, 2024
Complete
Visit 2 — Baseline
Feb 26, 2024
Complete
Visit 3 — Treatment
Window: Mar 11 – Mar 18
In Window
Visit 4 — Follow-up
Window: Mar 25 – Apr 1
Upcoming
Visit 5 — End of Study
Window: Apr 8 – Apr 15
Upcoming
Under the Hood

Everything you need for digital source

Purpose-built capabilities for clinical trial source documentation

Source Documentation

Configurable Source Forms

Design source forms that mirror your protocol visit schedule. Drag-and-drop fields, conditional logic, and edit checks — all without writing code.

Real-time Validation

Range checks, cross-field validations, and protocol-specific edit checks fire as data is entered — catching errors before they become queries.

Visit Schedule Management

Protocol-defined visit windows enforced automatically with overdue alerts, deviation tracking, and dynamic schedule views.

Data Integration

EDC Auto-Population

Source fields are mapped to EDC CRF variables. Data flows automatically with bidirectional sync and conflict resolution rules.

Query Management

Monitors raise queries against source data inline. Coordinators respond with corrections that update both source and EDC simultaneously.

Complete Audit Trail

Every data point is traceable: who entered it, when, from what source, and every change ever made. Tamper-evident audit logs included.

Compliance & Monitoring

21 CFR Part 11 Compliance

Full compliance with electronic signatures, reason-for-change capture, and certified PDF export for inspections.

Remote Source Verification

Side-by-side source and CRF views let monitors complete SDV remotely, flag discrepancies, and resolve queries from anywhere.

Native eSignatures

Execute 21 CFR Part 11 compliant sign-offs directly on the source form level, integrated into your audit trail.

Compare

Leave paper source in the past

See why leading sites and sponsors are moving to digital source with Clincove

FeaturePaper / Legacy SourceClincove SMR
Data CapturePaper worksheetsDigital source forms
TranscriptionManual re-entry into EDCZero — auto-populates EDC
Source VerificationOn-site binder reviewRemote SDV, side-by-side
Audit TrailPaper logs & manual trackingAutomatic, tamper-evident
Query ResolutionDays to weeksReal-time, inline
Setup Time6-10 weeks2-3 weeks

Have Questions?

Have questions about Clincove? We're here to help you find the right solution for your clinical trial needs.

Personalized platform walkthrough
Discuss your specific trial needs
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FDA 21 CFR Part 11
HIPAA & GDPR compliant
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