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Clinical Trial Platform for Real World, Late Phase Clinical Trials

Baseline Plus by Cisiv - intelligent technology, specifically designed for the unstructured nature of late phase and real world clinical trials

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Market leading late phase and real world clinical trial technology, developed by late phase experts.

Our cutting edge technology, Baseline Plus, is the only single end to end clinical trial platform specifically designed to meet the unique and complex nature of late phase studies. We collaborate directly with each of our clients to deliver innovative solutions, specifically tailored to meet your unique study requirements. Trusted by pharmaceutical and biotech organisations across the globe, we can deliver rapid study builds, suitable for any regulatory setting, which improve operational efficiencies, enabling you to deliver better data, faster.

Benefits of Baseline Plus for real world clinical trials

Highly flexible, fully integrated platform

One single clinical trial platform, specifically designed for late phase and real world clinical research.

Tailored to the specific needs of your late phase clinical trial

Our flexible technology can support any late phase, real world study design. Baseline Plus enables you to capture, access and manage late phase, real world study data without the need for multiple systems.

One solution for EDC, ePRO and eConsent

Baseline Plus contains EDC, ePRO & eConsent within one easy to use platform, removing the need to introduce physicians and patients to a variety of different systems.

Building long lasting relationships with the biggest pharmaceutical and CRO's across the globe

Collaborating with 90% of the top global pharmaceutical companies

OVER 200 studies delivered in the last 4 years

Proven to reduce data management costs by over 60%

Proposal Form

By providing us this information, one of our team of experts will be in touch with a no obligation proposal. However, if you would prefer to speak to someone directly, please email:

Baseline Plus is fully compliant with all global requirements for clinical systems including 21 CFR Part 11, GCP, GDPR, HIPAA