Better Site-Sponsor Relationships
For the Investigator
For the Sponsor
Reduced Administrative Burden
Reduced Cycle Times
Enhanced Trial Experience
Increased Compliance
Better Focus on Patient Safety
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Complete Oversight
Digitized Trials
Continuous Improvement
No more paper notifications to receive, sign, return, and track
Use a single sign-on and consistent safety letter solution
Acknowledge a single event notification per molecule across studies
See the medical significance of safety events more clearly
Enable distribution rules, create and distribute safety notifications within seconds
Bring workflow, data, reporting and visualization into a single intuitive solution
Build an integrated data experience that eliminates paper processes and informs future site selection
Standardize on a global solution that adapts to country, study, and site requirements
