eClinical Solutions is described as a clinical data platform that pulls many sources together for review and analytics. Capture sits earlier in the chain: the system where the study data is captured. This page helps you decide which problem you actually have.
Free sandbox · No credit card · 21 CFR Part 11 compliant
| eClinical Solutions | Capture | |
|---|---|---|
| Primary job | Ask vendor: data aggregation, review, analytics | Capture study data at the source |
| Sites enter data directly | Ask vendor | Yes, eCRF, ePRO and eConsent |
| One audit trail from entry | Ask vendor | Yes, field-level, append-only |
| Hands-on trial before contract | Ask vendor | Free sandbox |
| Priced in writing for your scenario | Request quote | Pricing page |
The short version
Two layers
A clinical study produces data in several places: the EDC, a central laboratory, imaging reads, wearables, a safety database and operational trackers. An aggregation or clinical data platform is aimed at bringing those feeds into a single reviewable store so that data managers, medical reviewers and statisticians see one picture. That is the space eClinical Solutions describes for elluminate in its press material.
A data capture system is where primary data is born. Sites key visit data, participants complete questionnaires and sign consent, and every entry is time-stamped, attributed and reasoned. Capture does this in one platform, so the audit trail starts at entry and does not need to be stitched across modules.
For a single early-phase study or a small portfolio, the capture layer is usually the first decision and the aggregation layer is a later one, if it is needed at all. For a sponsor running many studies with many external data vendors, the order can flip. Both situations are legitimate, and the questions below are designed to tell them apart.
Capture does not claim to ingest and harmonise arbitrary third-party feeds, and this page does not suggest it replaces an aggregation platform. It offers CSV and Excel exports with a data dictionary, and SDTM datasets as SAS XPT files with Define-XML, so data can leave Capture in structured form for whatever sits downstream.
Evaluation
Send the same list to each vendor and keep the answers in writing. Vendor columns are deliberately left for you to fill in.
| Topic | Question | What Capture offers for comparison |
|---|---|---|
| Scope | Which parts of our data flow does this product own: capture, aggregation, review, analytics, monitoring? | Capture owns capture: eCRF, ePRO, eConsent, randomization, queries and the audit trail. |
| Sources | Which of our data sources can it take in, how, and who builds each feed? | Data entered in Capture is already in one study. Ask any aggregation vendor for the feed list in writing. |
| Provenance | Can we trace a number in a report back to who entered it, when, and what it replaced? | Field-level audit trail with user, timestamp, old value, new value and reason; append-only and exportable. |
| Cleaning | Where are queries raised and answered, here or in the source system? | Edit checks raise auto-queries at entry; one query list with status and priority. |
| Validation | What validation documentation supports our own validated use? | Enterprise customers receive documentation to support sponsor validation and UAT; ask for scope. |
| Time to first use | How long from signature to a working environment on our protocol? | Sign up, build or upload the protocol for an AI draft, test in the free sandbox before going live. |
| Exit | What do we receive at lock and if we leave? | CSV/Excel with data dictionary, audit trail export, SDTM as SAS XPT with Define-XML. |
| Total cost | What are all charges over 24 months for our studies? | See the pricing page for current terms; ask others for equivalent detail. |
Capture rows come from the Capture product pages. Do not read the empty vendor side as a statement about eClinical Solutions.
Upload your protocol to the free sandbox, review the AI draft, and enter sample data. No card, no time limit.
Provenance
Whatever platform later combines your sources, its numbers are only as defensible as the capture step beneath them. In Capture every field change is written by the database with the user, time, previous value, new value and a reason, and the trail cannot be edited through the interface. That gives anyone downstream a clean record to join to.
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
Where the work happens
Decision aid
Start with a capture system. Test Capture in the sandbox before any aggregation purchase.
An aggregation platform is the relevant comparison; ask for your CRO's feed list.
Weigh the cost and setup of a second layer against exports from a single system.
Prefer a platform where ePRO and eConsent are native to the study.
Check export structure first: CDISC SDTM export software.
Process
List every source in your study and who owns it. This shows whether you have a capture problem, an aggregation problem or both.
Build one visit in the Capture sandbox with an edit check and a calculated field, and time it.
Send the table above to each vendor, then compare scope, time to first use, exit and 24-month cost.
Partly. Capture is a data capture platform (EDC, ePRO, eConsent, randomization). eClinical Solutions describes elluminate as a platform that aggregates and analyses data from many sources. They overlap only where a team might use a platform to review study data; they sit at different layers.
It is the clinical data platform from eClinical Solutions. According to the company's own materials it consolidates clinical and operational data and offers review and analytics components. Product naming has changed over time, so confirm the current line-up with the vendor.
No. They are different companies with different products. We have a separate page on eClinicalOS alternatives.
You can export CSV or Excel files with a data dictionary, raw and decoded, and SDTM datasets as SAS XPT with Define-XML. Confirm with the receiving platform which format it expects.
We do not quote competitor pricing because it is not published in a form we can verify. Ask for a written quote for your scenario.
Capture is ISO 27001 certified, 21 CFR Part 11 compliant, GDPR compliant, HIPAA compliant and ICH GCP E6(R3) compliant, with EU and US data hosting. The sponsor still owns validated use of the system for its studies.
Yes. The free sandbox includes the full feature set with no credit card and no time limit. You pay only when you go live with real participants.
Build a study in Capture, free. No credit card.