Collaborate and Write
Author protocols for Phase 2 and 3 IND-IDE studies as well as behavioral and social sciences research involving humans. Assign writers and reviewers to individual protocol sections.
Write · Review · Export
A structured workspace for protocols and informed consent forms
Build your study team, assign sections to authors and reviewers, and move each section from draft to approved — then export the assembled document for external review.
Track Progress
Track writing and reviewing progress across every section. Your team is alerted the moment a section is marked ready for review.
Export Protocol
When writing is finished, export the complete and final protocol and consent form for external review, including submission to ClinicalTrials.gov.