Pathways

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) 

Sample tracking ID generated for time points, sample etc

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.