Customer Voice

We are working on the next release of our Clinical Study Report platform, and want to know what you
would look for in this next release. 

Please complete the form below to rank the features that we are considering implementing. If there
are other features that would help you write your next Clinical Study Report that we aren't thinking of,
let us know! We appreciate your valuable feedback. 

Name
Name
Please rate the following features being considered for the next release of our CSR platform.
Please rate the following features being considered for the next release of our CSR platform.
To what extent do you agree or disagree that each of the following features are important to you?
Integrated SAS output into in-line tables, Section 14 Tables, Listings, and Figures, and Section 16 appendices.
Integration with Medical Device Reporting safety database to confirm reportable safety events have been filed.
Automatic extraction of Section 9 Investigational Plan details from uploaded clinical study protocol (i.e., inclusion/exclusion criteria, determination of sample size).
Direct references to TFLs to eliminate retyping and potential transcription errors.
Enhanced text editor including automatic hyperlinking and referencing to appendices.
Integration into Right Submission's 510(k) platform.
Sample suggested content for each section.
Document upload via integration with RIM Systems.
What should we be thinking about that we aren't?