Comparison · iMedNetUpdated September 29, 2026

Capture vs iMedNet: who builds your study, and how fast

iMedNet is an established eClinical platform used by sponsors and CROs, including in device studies. Capture puts the build in your team's hands with AI drafting, and combines EDC, ePRO, eConsent and randomization.

  • Free sandbox, no sales call
  • EDC, ePRO, eConsent, randomization
  • Part 11-aligned controls

Free sandbox · No credit card · 21 CFR Part 11 aligned

Evaluation · iMedNet vs Capture

Tests

5

Hands-on

4

To confirm

1

  • Rebuild one of your real formsSame test, both systems
  • Break an edit check and follow the querySame test, both systems
  • Complete a questionnaire on a phoneSame test, both systems
  • Sign a test eConsentSame test, both systems
  • Compare total cost for your studyAsk both vendors
Test both on your own protocol

Capture vs iMedNet: the short version

  • iMedNet is the eClinical platform from MedNet Solutions, including EDC.
  • iMedNet is used by sponsors and CROs across drug and device studies.
  • The key differences to test are build ownership, amendment speed and which modules sit in the same study.
  • Capture drafts the study from the protocol with AI and locks approved forms, so amendments are deliberate and recorded.
  • Capture supports device studies, with custom device deficiency forms and long post-market follow-up.

0

sales calls needed to start building

1

audit trail across EDC, ePRO, eConsent and randomization

Free

sandbox with every feature, no time limit

EU + US

hosting in Frankfurt or N. Virginia

The comparison

Build ownership and amendments

In some eClinical models the vendor or a services team builds the study; in others the sponsor does. Neither is wrong, but they lead to very different amendment experiences. When a protocol changes, who makes the change, how long it takes and what it costs decide how painful mid-study changes are.

In Capture, your team makes the change in the visual builder, tests it, and approves it. The audit trail records what changed. For device studies, see ISO 14155 and EDC and EDC for medical device trials.

What to compare

What to test when comparing Capture and iMedNet

CriterionWhy it mattersCapture
Build ownershipSpeed of builds and changesYour team builds; AI drafts from the protocol
AmendmentsTraceable changesDraft and approved states; approved forms locked; changes recorded
Modules in one studyReconciliation and vendor countEDC, ePRO, eConsent, randomization and kits with one audit trail
Device studiesDeficiencies and follow-upCustom device deficiency forms; long follow-up with remote questionnaires
Compliance controlsPart 11 and GCP expectationsField-level audit trail, re-authenticated e-signatures, role-based access
Commercial modelFit for your study sizeFree sandbox; no setup fee; pay only when you go live

This table shows Capture's answers only. Ask iMedNet for theirs, and confirm current capabilities and terms directly with them.

Self-serve build

Your team builds and amends, with AI doing the drafting

The AI form builder drafts questions or lab tables from a description or an uploaded file, and the AI Study Generator drafts the schedule from your protocol. Nothing is saved without human review. Forms move from draft to approved and are locked for live use, so amendments are deliberate and recorded.

  • Ten question types plus repeating table sections.
  • Calculated fields such as BMI, BSA, eGFR and QTc.
  • Configuration export and import between studies.
CRF builder for clinical trials
Build this form with AI

Question form

CRF or ePRO

Lab table

Analytes, units, ranges

Vital signs form: BP, pulse, temperature, respiratory rate, weight
Upload CSV, XLSX, PDF or DOCX
14 questionsReview before applying
  • 1. Systolic blood pressure

    Required · Number · mmHg · 0 dp

    Number
  • 2. Diastolic blood pressure

    Required · Number · mmHg · 0 dp

    Number
  • 3. Pulse rate

    Required · Number · beats/min

    Number
  • 4. Body temperature

    Required · Number · °C · 1 dp

    Number
  • 5. Position during measurement

    Required · Sitting, Supine, Standing

    Single choice
  • + 9 more questions
Back Apply to form

One platform

EDC, ePRO, eConsent and randomization in one study

Sites enter data on locked, approved forms with edit checks that raise queries at entry. Participants complete questionnaires on their own phones and sign eConsent with verified signatures. Randomization and kit management run in the same study, and everything shares one field-level audit trail.

  • One participant record across every module.
  • No integrations to build or reconcile.
  • Phase 1 through Phase 3.
EDC for Phase 3 clinical trials
app.capture.study · Dashboard
Capture study dashboard with enrolment, compliance, safety overview and site risk monitor

Build the same form in Capture

Free sandbox with every feature. No credit card.

Compare it free in the sandbox

Fit

When iMedNet fits, and when Capture does

iMedNet is often a good fit for teams with existing iMedNet studies and processes, and for organisations that prefer the vendor's build and support model.

Capture fits teams that want to build and amend studies themselves, with AI drafting, and run EDC, ePRO, eConsent and randomization in one study.

Compliance controls

The controls inspectors look for, built in

Every change is written to an append-only, hash-chained audit trail with user, time, old and new value and reason. Electronic signatures require password re-authentication and carry a meaning statement. Roles separate sites, and identifying data is segregated from study data at the database layer.

  • Field-level audit trail, never hard deleted.
  • Re-authenticated e-signatures.
  • Role-based access with site separation.
21 CFR Part 11 compliant EDC

Weight changed 68.0 to 68.5 kg

Site coordinator · Reason: Transcription error

9f2c…a71e

Query Q-0014 answered on Weight

Site coordinator · Reason: Source checked

4b8d…c203

Vital signs form locked

Data manager · Reason: Visit cleaned

e61a…58f0
Verify chain Intact

Switching

Moving from iMedNet to Capture

Start new studies in Capture with AI-drafted builds from the protocol or your existing specifications. Use the template library for standard forms.

Historical data stays in its original export and is combined at analysis if needed. See how to switch EDC vendors mid-study for when a mid-study move makes sense.

Evaluation

How to compare EDC vendors side by side

Same form in both systems

Build one real form with edit checks.

Site workflow

Enter data, raise and answer a query.

Participant workflow

Consent and a questionnaire on a phone.

Monitoring

Set SDV and review what a monitor sees.

Exports

Data dictionary, codes and labels.

Total cost

Setup, per-site and per-participant fees.

All comparisons

Compare Capture with other platforms

Every comparison uses the same approach: what to test, where each option fits, and Capture's own answers. See all of them on the comparisons hub at /compare.

FAQ

Questions teams ask before they switch

Something not covered here? Ask us directly.

Is Capture an iMedNet alternative?

Yes, for teams that want a self-serve build with AI drafting and EDC, ePRO, eConsent and randomization in one study.

Does Capture support medical device studies?

Yes. Build device and deficiency forms alongside the AE form and SAE workflow, with long post-market follow-up.

Who makes amendments in Capture?

Your team, in the visual builder. Approved forms are locked and changes are recorded in the audit trail.

Can I test Capture before deciding against iMedNet?

Yes. The free sandbox includes every feature with sample data, no credit card and no time limit. You pay only when you go live.

How did you build this comparison?

From public positioning and the criteria teams tell us matter. We state only Capture's own capabilities as fact; confirm iMedNet's current offering with them.

Compare Capture against your shortlist

Free sandbox with every feature. No sales call.

Compare it free in the sandbox