Trial Interactive’s e-feasibility streamlines the global feasibility process for deciding which countries should be in a study based on the disease prevalence, access to patients, regulations, and more. Feasibility can also be conducted at a potential site via questionnaires.

Trial Interactive will reduce administrative time for your investigative sites and data mine for future studies. Our e-feasibility solution eliminates site identification questionnaires from the process. The investigator database allows auto-population and storage of key investigative site information, such as ethics committee dates. The workflow allows for rapid review and approval, as well as email notifications of participation status. Trial Interactive can eliminate the need to request duplicate information.

Protocol feasibility assessment has traditionally meant asking key opinion leaders and scientific advisory boards about the medical feasibility and scientific soundness of the protocol. Sponsors obtain little or no input from the investigators and study coordinators who will eventually conduct the study.

Expecting sites to submit a questionnaire that demonstrates their ability to conduct a study and simultaneously gives thoughtful and honest feedback proves to be difficult – resulting in site selection processes to fail.

Feasibility Assessment is integrated with our Study Start Up module and our electronic Trial Master File solutions. TransPerfect’s e-feasibility solution allows investigators to populate information into a web survey, then relaying the information to the investigators. These surveys can be done completely online or they can be printed out and done in hard copy, and uploaded via email or fax upon preference.

To find out more about how Trial Interactive can streamline your global feasibility process, contact us.

Recent Updates and Improvements

  • CDA E-Signature Solutions:
    Users can use a built-in signature solution or integrate their DocuSign account with e-feasibility allowing for a more customizable CDA document as well as e-signature capture.

  • Section Based Questionnaire:
    Allows more customization for a personalized questionnaire. Users can now group similar question types into sections that are structured into different pages.

  • Auto Saving Response functionality:
    Every response, edit, and update is captured automatically. Users do not have to worry about data getting lost and Investigators do not have to re-do submissions.

  • Question Title Editing:
    Titles become editable for published questionnaires.

The Trial Interactive platform complies with all current and emerging regulations
including 21 CFR Part 11, ERES, ANNEX 11, GxP, and GDPR.

Reduction in
Feasibility Creation Time

Reduction in
Site Response Time

Reduction in
Review Time

Automate the manual processes associated with site feasibility questionnaire creation, submission, and warehousing

data entry translation

Enable easy online data entry and survey / questionnaire submission

paperless Study Start-Up

Go paperless and store document copy uploads in the cloud

eTMF Solutions

Integrate with our Study Start-Up and eTMF Solutions


Handle CDAs within the module from start to end

Single Sign-On

Secure single sign-on access

Contact us to learn more about our solutions

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