A giant leap forward for clinical trials
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Faster amendments with more flexibility
New tools for quality control and regulatory submission
Powerful tools for site settings and site-user access control
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Study Operations
Sponsor Oversight
Robust data on patient behavior down to the document and section levels
Access controls for remote monitoring or site visits
Peerless data quality regardless of location or language
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Single sign-on available for all non-patient users
Ultimate flexibility around document collections, and workflows to consent, reconsent, or withdraw from the first document version through the final amendment
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Site Satisfaction
Site Satisfaction
Sponsor Oversight
Study Operations
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