Trial Interactive will reduce administrative time for your investigative sites and data mine for future studies. Our
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
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.
Feasibility Creation Time
Site Response Time
Automate the manual processes associated with site feasibility questionnaire creation, submission, and warehousing
Enable easy online data entry and survey / questionnaire submission
Go paperless and store document copy uploads in the cloud
Integrate with our Study Start-Up and eTMF Solutions
Handle CDAs within the module from start to end
Secure single sign-on access
Contact us to learn more about our solutions