Clinical trial sites tell us that they are consistently expected to do more with less. Large volumes of documents must be read, understood, and signed off on by all site staff participating in day to day trial activities, but how can site staff effectively and efficiently manage and review this continual influx of documentation designed to support them in their work?
Our simple design allows access to documents on a role, region, site, functional group and/or user level. Key documents can also be flagged as mandatory by the study team and tracked via electronic signature. Folders and sub-folders can be created by sponsors to maintain naming conventions and consistency with the eTMF.
We have engineered our platform so that study team delegates can directly manage document and alert distribution to site staff themselves without external support. Study teams will also have access to ‘real-time’ oversight dashboards and reporting functionality.
Guided Compliance™ delivers the right resources at the right time to your site staff, making compliance instinctive, so they can focus on patients.
Fill out the form to sign up for a demonstration. One of our specialists will follow up to schedule a one-on-one overview of the technology.