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 credit card · 21 CFR Part 11 aligned
Tests
5
Hands-on
4
To confirm
1
Capture vs IQVIA: 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
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
| Criterion | Why it matters | Capture |
|---|---|---|
| Platform ownership | Who controls the build and data | The sponsor owns the study; CROs work in it with assigned roles |
| Reuse | Building the next study faster | Configuration export and import between studies |
| Modules | ePRO, eConsent and randomization | All in one study with one audit trail |
| Exports | Changing providers later | CSV and Excel with a data dictionary, raw and decoded |
| 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 IQVIA for theirs, and confirm current capabilities and terms directly with them.
Speed to start
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.

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.

Upload a protocol to the free sandbox and compare the draft.
Fit
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
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
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
Ask each vendor to build one real visit, not a demo study.
Contract, build, testing and training, in weeks.
EDC, ePRO, eConsent and randomization: one or several?
Who changes a form, and how long it takes.
Change a value and read the record.
Setup, licences, per-site fees and change orders.
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 sponsors who want to own their study platform and let any CRO or in-house team work in it.
Yes. Invite CRO staff with the roles they need, such as monitor or data manager.
Yes. Many teams build and run studies themselves in Capture. See how to run a clinical trial without a CRO.
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 IQVIA's current offering with them.
Keep exploring
IQVIA EDC alternatives
A broader alternatives guide.
Data ownership and portability
Keep your data portable.
Capture vs Medidata Rave
Enterprise EDC from Medidata, part of Dassault Systèmes.
Capture vs Veeva Vault CDMS
Vault EDC and CDMS within Veeva's clinical platform.
Capture vs Oracle Clinical One
Oracle's unified clinical platform and InForm heritage.
Capture vs Merative Zelta
Formerly IBM Clinical Development.
Free sandbox with every feature. No credit card, no sales call.