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Clinical Trial Platform for Phase IV Clinical Trials

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

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Tailored and flexible solutions that support the complex nature of phase IV clinical trials

Phase IV and real world studies are complex and unstructured and there is an increasing requirement for flexible technology which can meet the unique nature of these study designs. Our cutting edge technology, Baseline Plus, is the only single end to end clinical trial platform, specifically designed to meet the unique needs of phase IV and real world research studies. We collaborate directly with each of our clients to deliver innovative solutions which are tailored to meet your unique phase IV study requirements. Trusted by over 200 pharmaceutical and biotech organisations, we can deliver rapid study builds, suitable to any regulatory setting, which improve operational efficiencies, enabling you to deliver better data, faster.

Benefits of Baseline Plus for phase IV clinical trials

Highly flexible, fully integrated platform

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

Tailored to the specific needs of your phase IV clinical trial

Our flexible technology can support any phase IV, real world study design. Baseline Plus provides an end to end set of modules that plug into the varied designs found in phase IV studies, without the need for multiple systems.

Technology that enables both patient and physician engagement

Baseline Plus contains eCOA, ePRO, eConsent and eDiary modules enabling data from patients and physicians to be captured in one place.

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

Collaborating with 90% of the top global pharmaceutical companies

Supporting OVER 200 Pharma/Biotech companies

Proven to reduce data management costs by over 60%

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Book a demo now to speak with one of our late phase experts about how Baseline Plus can help you build more dynamic and comprehensive late phase studies.

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