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 credit card · 21 CFR Part 11 aligned
Tests
5
Hands-on
4
To confirm
1
Capture vs iMedNet: the short version
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
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
| Criterion | Why it matters | Capture |
|---|---|---|
| Build ownership | Speed of builds and changes | Your team builds; AI drafts from the protocol |
| Amendments | Traceable changes | Draft and approved states; approved forms locked; changes recorded |
| Modules in one study | Reconciliation and vendor count | EDC, ePRO, eConsent, randomization and kits with one audit trail |
| Device studies | Deficiencies and follow-up | Custom device deficiency forms; long follow-up with remote questionnaires |
| Compliance controls | Part 11 and GCP expectations | Field-level audit trail, re-authenticated e-signatures, role-based access |
| Commercial model | Fit for your study size | Free 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
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.
Question form
CRF or ePRO
Lab table
Analytes, units, ranges
1. Systolic blood pressure
Required · Number · mmHg · 0 dp
2. Diastolic blood pressure
Required · Number · mmHg · 0 dp
3. Pulse rate
Required · Number · beats/min
4. Body temperature
Required · Number · °C · 1 dp
5. Position during measurement
Required · Sitting, Supine, Standing
One platform
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.

Free sandbox with every feature. No credit card.
Fit
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
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.
Weight changed 68.0 to 68.5 kg
Site coordinator · Reason: Transcription error
Query Q-0014 answered on Weight
Site coordinator · Reason: Source checked
Vital signs form locked
Data manager · Reason: Visit cleaned
Switching
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
Build one real form with edit checks.
Enter data, raise and answer a query.
Consent and a questionnaire on a phone.
Set SDV and review what a monitor sees.
Data dictionary, codes and labels.
Setup, per-site and per-participant fees.
All comparisons
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.
Yes, for teams that want a self-serve build with AI drafting and EDC, ePRO, eConsent and randomization in one study.
Yes. Build device and deficiency forms alongside the AE form and SAE workflow, with long post-market follow-up.
Your team, in the visual builder. Approved forms are locked and changes are recorded in the audit trail.
Yes. The free sandbox includes every feature with sample data, no credit card and no time limit. You pay only when you go live.
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.
Keep exploring
iMedNet alternatives
A broader alternatives guide.
EDC for medical device trials
Device studies.
Capture vs Castor
EDC, eCOA and eConsent from the Netherlands.
Capture vs Viedoc
EDC with patient modules, from Sweden.
Capture vs Medrio
EDC and eCOA for early-phase and mid-sized studies.
Capture vs OpenClinica
Cloud EDC with an open-source heritage.
Free sandbox with every feature. No sales call.