The Curebase platform empowers CROs to take charge of the study build with the most expansive participant-facing software feature set in the industry.
Get in touch with us to learn more about platform self-service options for CROs.
No matter the study, no matter the data, our platform makes it easy to collect participant data at every point in the study. From recruitment workflows and electronic consent to ePROs, notifications and more, Curebase has you covered.
The Curebase platform plays well with other data streams allowing you and your team total data dominance. Remote patient monitoring (RPM) technologies are becoming more commonplace while legacy EDC and IRT systems are still in use.
Curebase's platform can be easily integrated with other systems to reduce the technology burden on the participant, site and study teams.
We want our customers and users to have access to expertise on our software. Work with us to configure our platform the way you want for best in-class user experience workflow. Our team will also train your staff, sites, and other users on how to use our software. The process is easy to start and quick to complete.
Clinical trial platforms often lack self-service configuration, leaving sponsors and CROs without control over timelines and quality. Our certification program empowers users to create their ideal software, with support from Curebase study builders, as needed.
Different organizations have varying needs for clinical trial software. For those with fewer studies, we offer cost-effective single-study pricing. Larger organizations can benefit from unlimited builds, white labeling, dedicated support, and more.
You are the experts in the science. We’ve built world class best practices in patient and user experience. Combining the two on your protocol we help to enhance your study design for optimial recruitment, retention, and patient satisfaction. We handle all IRB submission both central and instiutional.
Our network consists of over 300 health care providers. We have experience with over 50 Principal Investigators of all backgrounds and experience levels. Couple this with our in house staff of clinical research coordinators, and conduct powerful studies that reach patients at academics, community PCPs, mobile providers, and many more.
We want our customers and users to have access to expertise on our software. Work with us to configure our platform the way you want for best in-class user experience workflow. Our team will also train your staff, sites, and other users on how use our software. The process is easy to start and quick to complete.
Make the most our of our seamless recruitment workflow by having us design and manage your recruitment campaigns. Our team works on building study brands, landing pages, and using digital and site based marketing to fully enroll your study.
We advise study teams and build patient communication plans that leverage a combination of automated and personal touch engagement techniques. Our SMS/email notifications and updates in addition to CRC outreach and support are available.
Project management should be easy and transparent. On each study our PMs build living timelines, provide access to real-time dashboards, and access to monitoring resources on studies. Leverage all or some of our traditional clinical operations functions to fully manage and monitor your study.
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Meet with us to learn how our platform can help make your study run smoother.