Connect with us to see how our pre-configured oncology eCOA can enhance your upcoming oncology trial.
TIMELINES
Data You Can Trust-
Delivered in the Time & Budget You Need
8 WEEKS
12 WEEKS
Pre-Configured Solution
Full Custom-Build
33% FASTER
Design & Implementation
20% SAVINGS
Compared to Custom eCOA
PAST 5 YEARS OF ONCOLOGY EXPERIENCE
STUDIES
PATIENTS
COUNTRIES
SITES
LANGUAGES
INDICATIONS
334
158,000+
67
44,000+
116
30+
Signant SmartSignals eCOA
A Leading Global eCOA Solution in Oncology Studies
Randomization and Trial Supply Management: to manage the complex study designs and medication supply-chains in oncology studies
Integrated activity and sleep monitoring: to measure the impact of acute treatments and measure recovery post-treatment
eConsent: to effectively convey complex study information and manage optional study components and re-consenting
Patient Concierge: Engage and retain patients during acute treatment and post-treatment follow up studies
Outcome analytics: Scientific data reliability and consistency monitoring using analytics and in-house algorithms.
Our oncology eCOA Package offers the best ability to capture reliable endpoint evidence that includes the features you need to increase speed, reduce cost, and ensure consistency across sites and geographies in less time.
At Signant, we’ve worked with sponsors for over 20+ years on oncology trials and understand the pain points and complexities they bring.
33% Faster Design
with an Average 8 Week Implementation
20% Savings Compared to Custom eCOA
20+ Years of Oncology Experience Built In
Part of Signant Health’s Suite
of Solutions for Oncology Trials