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.