CLINICAL TRIALS
A custom build platform to help you manage any clinical trial
Any range of complexity covered including blinding, sample tracking and multi-site trial co-ordination
OVERVIEW
Pathpoint
Bespoke platform for the unique requirements of a clinical trial using remote referrals from any number regional units to a central receiving hub or labs for biological samples.
Customisable pathways designed to deal with complex pathways and effective data collection.
FEATURES
Pathpoint capabilities
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Double blinding of referring patients identifying information to the hub/labs/clinical investigators keeping to study ethics and information governance policies
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Team based access to for different levels or access which can be controlled anytime
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Patient study number or clinical trial number auto generated
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Digital proformas for patient questionnaires either filled in digitally at source by patient on any web device or manually entered by clinical trial staff
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Digital clinical questionnaires or assessments to be entered by clinical staff
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​Sample tracking pathways for any biological sample (DNA,bloods, urine for example)
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Sample tracking ID generated for time points, sample etc
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Notification reminders for extra samples collections or assessments
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Fully coded fields for effective data collection for any fields
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Full data reports for audits, data analytic software
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Fully integratable with other healthcare systems (EPR, EMR, PAS,)
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PDF reporting for any pathways.
