
OVERVIEW
Pathpoint® Clinical TrialsÂ
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


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