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™ Clinical Trials 

Bespoke platform for the unique requirements of a clinical trial using remote referrals from any number of regional units to a central receiving hub or labs for biological samples. 

 

Customisable pathways designed to deal with complex pathways and effective data collection.

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FEATURES

Pathpoint™ capabilities
  • Double blinding of referring patients identifying information to the hub/labs/clinical investigators keeping to study ethics and information governance policies

  • Team based access to for different levels or access which can be controlled anytime

  • Patient study number or clinical trial number auto generated 

  • Digital proformas for patient questionnaires either filled in digitally at source by patient on any web device or manually entered by clinical trial staff

  • 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 

  • Fully coded fields for effective data collection for any fields

  • Full data reports for audits, data analytic software

  • Fully integratable with other healthcare systems (EPR, EMR, PAS,)

  • PDF reporting for any pathways.

ADDITIONAL RESOURCES

Learn more about how Pathpoint™ is helping NHS partners transform their workflows
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Pathpoint™ eDerma

Helping to meet increasing demand, reduce costs and develop a nurse-led triage service

Pathpoint™ eTrauma​

Revolutionising how the team manages its admissions and prioritises patients

Rapid Regional Care

The rapid delivery of Pathpoint™ eTrauma to manage regional trauma care seamlessly