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Increase
speed

to accelerate eCOA and IRT implementation.

Empower
flexibility

to support your clinical trials through protocol
amendment. 

Inspire

certainty

to empower you with better clinical trial outcomes.

Unmatched, 100% configurable, no-code eCOA platform reduces launch times by up to 47%.
Industry-leading IRT platform enables accelerated protocol amendment edits, improving study timelines.
Intuitive eConsent makes enrollment seamless, driving compliance and ease for patients and sites alike.
%
faster
X
swifter
%
configurable
Optimize clinical trial processes.
Customize data collection.
Seamlessly integrate systems.
Gain actionable insights to improve decision making.
Optimize clinical trial processes.
Customize data collection.
Seamlessly integrate systems.
Gain actionable insights to improve decision making.
No other data science team at any other eCOA company helps construct data standards for my studies.
 – Top 15 Pharma Customer
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