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.
Feasibility Creation Time
Site Response Time
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