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CLINICAL TRIALS

A custom built platform to help you manage any clinical trials including blinding, sample tracking and multi site trial coordination. 

OVERVIEW

Pathpoint® Clinical Trials 

A bespoke platform built for the unique requirements of any clinical trial  

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Customisable pathways designed to deal with complex workflows and facilitate effective data collection

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Allows for easy collection of biological samples from regional units

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FEATURES

Pathpoint® capabilities

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  • ​Sample tracking pathways for any biological samples (DNA, bloods, urine plus many more) 

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  • Sample tracking ID generated for time points

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  • Notification reminders for extra sample collections or assessments 

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  • Fully coded fields for effective data collection

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  • Full data analysis and reports for auditing purposes

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  • Fully interoperable and integrates within existing technology ecosystems

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  • Meet Information Governance Standards and align with the ethics policy with easy double blinding of referring patients

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  • Controlled, team-based access across different levels

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  • Automatically generated patient and study number

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  • Digital patient questionnaires and direct patient communication tools

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