Vendor comparisonUpdated October 18, 2026

ClinPlus alternatives: how to judge a CTMS-rooted EDC suite

ClinPlus is described in public listings as an eClinical platform that combines EDC with trial management, eTMF and randomisation. This page sets out what those listings say, the questions to put to the vendor, and when a focused self-serve EDC is the better test.

  • Listing-based, hedged
  • One-week evaluation plan
  • Who should stay

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

A one-week side-by-side evaluation · demo plan
1234567

days

Freeze the protocol excerpt

Same 6 forms for every vendor

Build in vendor A (demo)
Build in Capture sandbox

Free, no card

Enter 10 test participants
Score and decide
Demo plan, not a measured benchmark of any vendor.

What to know first

  • What listings say: ClinPlus EDC is described as the data capture part of the ClinPlus Clinical platform from DZS Software Solutions, with CTMS, eTMF and IWRS on the same platform. Press material says EDC features were added to an existing web-based CTMS, and the vendor describes audit trails and electronic signatures aligned to 21 CFR Part 11. Directory pages list cloud delivery and English. All of this is third-party or vendor-sourced and should be confirmed.
  • What we do not claim: anything about ClinPlus pricing, validation documents, service levels, customers or product roadmap. Directory price figures change and are not repeated here.
  • The core question is scope. A platform that began as CTMS and added EDC may suit a team that runs operations and data in one place. A team that mainly needs fast, well-controlled data capture may want a focused tool.
  • Test both the same way: one protocol excerpt, same forms, same checks, same ten test participants. Capture has a free sandbox for this, with every feature and no credit card.
  • Capture is suitable for Phase 1 to 3, with EDC, ePRO and eConsent in Core and eTMF and CTMS in Full Platform.

The vendor

What is publicly described about ClinPlus

ClinPlus appears in vendor press releases and software directories as the ClinPlus Clinical Platform, offered by DZS Software Solutions, with a parent company listed as Anju Software. The product is described as a single web platform in which data capture sits alongside clinical trial management, trial master file and randomisation and supply modules. A directory FAQ calls the EDC the data-capture component of that suite, and a vendor release describes replacing separate EDC and CTMS integrations with mapping inside one product.

None of that is a verdict. Listings are marketing, directories can merge or mislabel products, and some pages for this vendor appear under other product names. Confirm the product, owner and current version with the vendor before you compare anything. For the checks that apply whichever vendor you choose, see the EDC vendor audit checklist and the 21 CFR Part 11 compliance checklist. Part 11 is shared between the software and your own validated use of it, so a vendor statement is the start of qualification, not the end.

Decision matrix

Ten questions, asked of ClinPlus and Capture alike

The ClinPlus column is a question to put to the vendor, not an answer. Capture's column is from its published product and pricing pages.

QuestionAsk ClinPlusCapture's answer
Can we try the real product before a sales call?Ask whether a trial or sandbox exists and what is restricted in it.Yes: free sandbox, every feature, no credit card, no time limit.
Which modules are in the quote?List EDC, CTMS, eTMF, IWRS separately and ask which are licensed together.EDC, ePRO and eConsent in Core; eTMF, CTMS, stratified/blinded randomisation and drug supply in Full Platform.
Who builds and amends the study?Vendor team, partner, or your team? Get change turnaround in writing.Your team, with an AI study builder that drafts visits and forms from a protocol for review. Setup by the Capture team is $0 on Core per the pricing page.
Published price?Ask for a written quote including change orders.Core $1,000/month incl. one live study + $50 per participant per month; Full Platform $5,000/month + $30; Enterprise custom.
Edit checks and queriesAsk for a demo using your own range rules.Range high, range low and custom value checks raise an auto-query at entry.
Audit trailAsk for a sample export.Field-level: user, time, old value, new value, reason; exportable.
Data outputsAsk about SDTM, Define-XML and interim exports.CSV/Excel with data dictionary; SDTM as SAS XPT with Define-XML.
LanguagesListings mention English; confirm what you need.No multilingual claim is made here; confirm your needs on a demo.
HostingRegions and residency.EU (Frankfurt) or US (N. Virginia).
ExitExport format and exit fee.CSV/Excel and audit trail export; confirm contract terms.

Run your six-form excerpt in the Capture sandbox

Upload the excerpt, let the AI draft visits and forms, edit them yourself and enter ten test participants. Every feature, no credit card, no sales call.

Build your study free

How to evaluate

A fair one-week test for any EDC suite

The point is to compare experience on identical work, not to read feature lists.

  1. 1

    Pick a protocol excerpt

    Six forms is enough: demographics, vitals, one lab table, adverse events, concomitant medications and one scale. Include one repeating section and one dependent field.

  2. 2

    Write five edit checks before you start

    For example a systolic blood pressure range, a visit-date window, a start date that must follow the consent date. Ask each vendor to build the same five.

  3. 3

    Time the first build honestly

    Note who did the work (you or the vendor), how many round trips it took, and what you could change yourself afterwards.

  4. 4

    Enter ten test participants as three roles

    Act as a site coordinator, then a monitor, then a data manager. See how queries are raised, answered and closed.

  5. 5

    Export and read the audit trail

    Pull the data and the trail. Check the codebook, units and change reasons. See audit trail software for clinical trials for what to expect.

  6. 6

    Price the whole scenario

    Use the EDC quote request template so each reply lists setup, subscription, per-participant, module and change-order lines.

Fair view

Who should stay with a suite, and who should look elsewhere

Stay if your team already runs studies on ClinPlus, the build is validated, and operations staff rely on CTMS and eTMF in the same system. Switching a live study is a project with its own risk; see how to switch EDC vendors mid-study. Plan a change for the next study, not the current one.

Look at an alternative when the next study needs a quicker first build, when you want published prices to benchmark quotes, or when you want ePRO and eConsent inside the same audit trail as the EDC. Teams unsure whether they need operations modules at all should read EDC vs CTMS and EDC vs eTMF first; many small studies need less than a full suite. For the labour side of the decision, see self-serve vs full-service EDC.

Where Capture fits

Data capture first, with operations modules when you need them

Capture starts with the study data and the people entering it. When the study grows into trial master file and site management needs, Full Platform adds eTMF and CTMS without a second vendor.

  • Forms move from draft to approved; approved forms are locked for live use.
  • Source data verification can be set per field.
  • Role-based access separates researcher, site coordinator and admin views.
  • Cost for a 500-participant example is worked in the 500-patient worksheet.
See the EDC product
Modules by plan
CoreFull Platform
EDC and eCRF builder
ePRO and eConsent
eTMF and CTMS
Stratified, blinded randomisation
Drug supply

FAQ

Questions teams ask before they switch

Something not covered here? Ask us directly.

What is ClinPlus?

According to public listings, ClinPlus is an eClinical platform from DZS Software Solutions that combines EDC with CTMS, eTMF and IWRS. Confirm product scope, ownership and current versions with the vendor.

What are good alternatives to ClinPlus EDC?

It depends on what you need. For a focused cloud EDC, teams commonly compare Viedoc, Castor, TrialMaster and Capture. Run the same excerpt through each rather than relying on feature lists.

Is ClinPlus 21 CFR Part 11 compliant?

Vendor press material describes audit trails and electronic signatures built for Part 11. Ask for documentation and a validation package, as you would for any EDC; compliance is shared with your own validated use.

How is Capture different?

Capture is a self-serve platform with a free sandbox, published Core and Full Platform pricing, an AI study builder and EDC, ePRO and eConsent in one system. We make no claims about ClinPlus pricing or services.

Does Capture have CTMS and eTMF?

Yes, on Full Platform. They are not in Core.

Should I move a running ClinPlus study?

Usually not. Start the next study on the new system and read the guide on switching EDC vendors mid-study if you must move.

Is Capture suitable for Phase 3?

Yes. Capture is suitable for Phase 1 to 3.

Put Capture next to your ClinPlus shortlist

Free sandbox with every feature. No credit card, no sales call, and you pay only once you go live.

Build your study free