Designed specifically for the communication needs and compliance requirements of life sciences and research facilities, Path eClinical™ reduces costs and maximizes efficiency by quickly connecting trial investigators in any location to improve retention and increase compliance.
Path Clinical™ adheres to industry compliance regulations including 21 CFR Part 11 for electronic records.
Increase information retention and improve investigator compliance by reducing lag time between training and trial launch.
Real-time insight to generate detailed reports, allowing you to accurately evaluate study performances.
Significantly reduce the costs of investigator training and increase efficiencies by connecting worldwide trial locations instantly via the web.
Allow study administrators to follow up training with assessment tools, including pre-, post-, and pop-up testing.
Create assignments, receive responses and provide feedback.
Get more from your Path eClinical™ tools
Utilize our integrations with Adobe Connect, Zoom, GoToMeeting and GoToWebinar. Participants seamlessly register with our integrated registration engine.
Quickly and easily integrate Path Clinical™ with your existing platforms including eTMF or other document management systems so users experience a single, streamlined sign-on.
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