Unified eClinical
eTrial design, EDC, SDV, coding, CDMS (for paper, electronic and hybrid trials) and reporting—all in one system, without hand-offs
On-demand, when you need it
Set up early phase studies with low overhead, initiate sites and scale capacity for late phase studies in line with enrolment, roll out protocol amendments without downtime or interruption
Anywhere you need
Operate electronically in sites with no high-speed Internet access and limited mobile coverage. Support large, global studies while maintaining fast validation check and page turn rates
At the push of a button
Modify pages, validation checks and data defintions; perform protocol amendments without interrupting sites. Add capcity; upgrade systems and perform maintenance without downtime
