Streamline data collection in clinical trials with eClinical

Most trials will involve a large number of participants, investigators and sites, so you have to be able to rely on the robustness of your data collection processes. The aim of eClinical is to create a process for data collection in clinical trials that is reliable, consistent, accurate and efficient.

Walk through the steps involved to get better grasp of what our data capture system can do for you.

Design

attractive and functional questionnaires, surveys and case report forms with the easy to use CRF designer module to meet trial protocol and standard operating procedures (SOP)

Capture

patient data whatever the method of delivery (fax, paper, web or eMail) for maximum efficiency

Extract

data using OCR, ICR, OMR, barcode, and logo recognition

Verify

the captured data for accurate and reliable results

Export

data to the Trial Master File (TMF), Clinical Trial Management Software (CTMS) or related databases and applications for true integration

Archive

and retrieve forms securely and conveniently for total accountability

You can also read our FAQ section.

If you want to learn more about hybrid paper and electronic data capture in clinical trials, or wish to book a demonstration, please contact us.

Next (Design)

Address: ePartner Consulting Ltd, PO Box 1578, Lightwater, GU20 5AR, United Kingdom. Tel: +44 (0)3300 100 000.

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