FAQ

This module may be made easily available to anyone who has access to the eTMF, Site or Study Collaborate rooms as well as a standard Content Management workspace.

During a Clinical Trial, so many questions come up from the team. These questions can range from document naming conventions, instructions on how to classify certain metadata and content, who to contact for specific study information, all the way to entries for each Investigative Site providing contact information and other critical information. If your CRAs, CTAs, and Clinical Document Specialists have access to the right answers your project can run much more efficiently. Simply click on the FAQ Module and take a look.