Integration EDC, eCOA & Site CTMS

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Integration EDC, eCOA and Site CTMS

Our CRF, TrialPal & PFS or Trial 360 combined 

The combination of three of our best solutions made to be an easy to use platforms for all the needs of your site.

Monitoring  of study participants and the study in general, minimizing processes, reducing costs, keep a tracking on diaries and registers, and also monitoring the information on a clinical study; all in one integration.

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With an initial study discount!

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Integration Model

Below you will find an integration example. Our solutions include an easy to configure API that extracts data from our ePRO or eCOA to Site CTMS and along with or CRF Importer is then transferred to our proprietary eCRF or to a third party study EDC system like RAVE. In the RAVE example we use Rave Web Services to make both systems communicate with each other. We have also developed an integration checker that review and compares data between systems, so the site can be confident that all data was transferred successfully and that data integrity is being met.


  1. Integrations take 2-3 weeks depending (approx) on study forms (# variables, visits, e-dairy days).

  2. Testing and validation takes 1 week (approx), to make sure integration works flawless.

  3. Rave dedicated user needed to authenticate transactions via RWS.

All digital, less time, save $

No more loss of information, no more hiring of digitization services, and no more human errors. Get savings. Allow remote access to CRAs. Be efficient

Customized stats

Real-Time with export to excel documents with customized stats and data

Get close to your patient or subject

Receive immediate notifications of any patient report, act quickly, gather insight and respond to study objectives. Use the end-user preferred communication method such as secure chat, schedule visits, and easily set up a new study within a couple of hours according to study protocol.


All your data completely secured and systems 21 CFR Part 11 Compliant

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If you want to know more about it


If you want to know more about how our systems are validated and comply with 21 CFR Part 11