Comparison · IQVIA EDCUpdated September 29, 2026

Capture vs IQVIA EDC: separate the platform from the service provider

When your CRO also provides the EDC, platform and service decisions are bundled. Capture lets sponsors own the study platform, invite any CRO to work in it, and keep data exportable whichever provider they use.

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

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

Evaluation · IQVIA vs Capture

Tests

5

Hands-on

4

To confirm

1

  • Build one real form from your protocolSame test, both systems
  • Time from contract to first site liveSame test, both systems
  • Check ePRO, eConsent and randomization togetherSame test, both systems
  • Export data with a data dictionarySame test, both systems
  • Compare total cost for your study sizeAsk both vendors
Test both on your own protocol

Capture vs IQVIA: the short version

  • IQVIA offers EDC and other clinical technologies as part of its technology portfolio, often alongside its CRO services.
  • IQVIA's technology is frequently used in studies where IQVIA also provides CRO services, which can simplify vendor management for sponsors who outsource broadly.
  • Sponsors compare alternatives when they want to own the data platform independently of their CRO choice, or run studies in-house.
  • Capture is CRO-independent: sponsors, CROs and academic teams can all build and run studies in it, and the sponsor keeps the data exportable.
  • EDC, ePRO, eConsent and randomization share one study and audit trail.

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

Separating the platform from the service provider

When a CRO also provides the EDC, the platform decision is bundled with the service decision. That is convenient, but it can make it harder to change CROs, bring work in-house or reuse a study build elsewhere. Some sponsors prefer to choose the data platform themselves and let CROs work in it.

Capture supports that model: the sponsor holds the study, CRO and site staff are invited with the roles they need, and data exports in open formats with a data dictionary at any time. Study configurations can be exported and imported into new studies. See EDC for CRO-independent trials.

What to compare

What to test when comparing Capture and IQVIA

CriterionWhy it mattersCapture
Platform ownershipWho controls the build and dataThe sponsor owns the study; CROs work in it with assigned roles
ReuseBuilding the next study fasterConfiguration export and import between studies
ModulesePRO, eConsent and randomizationAll in one study with one audit trail
ExportsChanging providers laterCSV and Excel with a data dictionary, raw and decoded
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 IQVIA for theirs, and confirm current capabilities and terms directly with them.

Speed to start

Build your study this week, before any contract

Upload the protocol and the AI Study Generator drafts the visits, windows and forms for your team to review. Refine them in the visual builder, test with sample data in the free sandbox, and export a blank eCRF PDF for ethics submission. You pay only when you go live with real participants.

  • AI-drafted visits and forms from your protocol.
  • Free sandbox with every feature, no credit card.
  • No setup fee and no sales call to start.
The fastest way to launch a clinical trial
app.capture.study · New study
Capture AI Study Generator: describe the study or upload a protocol to generate it

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

Run the same test in Capture today

Upload a protocol to the free sandbox and compare the draft.

Compare it free in the sandbox

Fit

When IQVIA fits, and when Capture does

IQVIA's technology is often a good fit when IQVIA is running the study as your CRO, when you want one provider accountable for both services and systems, or for very large programmes that rely on its global infrastructure.

Capture fits sponsors who want a platform of their own that any CRO or in-house team can use, and smaller studies where a self-serve build is faster than a service-led one.

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 IQVIA to Capture

Plan platform changes at study boundaries, and agree in CRO contracts which platform new studies will use. Export forms and specifications and let Capture's AI draft the new build for review.

Make exit terms explicit for every vendor: export formats, timelines and costs. See clinical trial data ownership and portability.

Evaluation

How to run a fair enterprise EDC evaluation

Use your own protocol

Ask each vendor to build one real visit, not a demo study.

Time the path to first site

Contract, build, testing and training, in weeks.

Count the systems

EDC, ePRO, eConsent and randomization: one or several?

Test an amendment

Who changes a form, and how long it takes.

Check the audit trail

Change a value and read the record.

Price your real study

Setup, licences, per-site fees and change orders.

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 IQVIA EDC alternative?

Yes, for sponsors who want to own their study platform and let any CRO or in-house team work in it.

Can our CRO work in Capture?

Yes. Invite CRO staff with the roles they need, such as monitor or data manager.

Can we run studies without a CRO?

Yes. Many teams build and run studies themselves in Capture. See how to run a clinical trial without a CRO.

Can I test Capture before deciding against IQVIA?

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 IQVIA's current offering with them.

See how fast your study can start

Free sandbox with every feature. No credit card, no sales call.

Compare it free in the sandbox