How eClinical Works: 5 simple steps to error-free clinical form and CRF processing

As a new drug or product development can take many years and cost millions, you cannot underestimate the importance of your document and form processing and archiving.

However big or small the trial, it is prone to human error. As many trials involve a large number of participants and investigator sites, you have to be able to rely on your collection processes.

The simplicity of eClinical is such that any member of staff with basic IT literacy skills can be trained up to take responsibility for form design and system administration.

Walkthrough the steps involved to get better grasp of what it can do for you.


  1. Design attractive and functional clinical trials forms with the easy to use design module
  2. Capture patient data however the method of delivery (fax, post, web or eMail) for maximum efficiency
  3. Verify the data for accurate results
  4. Export data to the Trial Master File, relevant databases or related applications for true integration
  5. Archive and retrieve forms securely and conveniently for total accountability


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