Helping life science CxO teams
outperform their competitors.

The Flaskdata platform: Patient-compliance automation in the cloud for clinical trials.



Provides an immediate picture of your study with continuous data feeds from EDC, patients, connected medical devices, mobile apps and wearables.


Reduces costly manual monitoring and sustains high rates of patient compliance to the protocol.

  • Automated deviation detection - 100X faster and a fraction of the cost of manual site monitoring.
  • Automated playbook response - alert the study team and reinforce patient compliance.
  • Real-time compliance posture in all study dimensions: subject, site, cohort, event, CRF, time.
  • Strong data security and privacy controls. HIPAA, GDPR and 21 CFR Part 11 compliance.
  • Flask API enables you to integrate devices, apps and information processing systems.
  • Fixed price subscriptions. Unlimited data and users.

Therapeutic areas

Patient compliance automation for clinical trials

Women’s reproductive health

Reduction of patient burden in a study and extremely fast detection of protocol deviations and adverse events are key to success in gynecology studies. The combination of low-touch data collection, passive sensors and real-time detection and response enables the executive team to perform studies on-time and under budget.

Patient compliance automation for clinical trials

Pain

The difference between a futile study and a successful one is the ability to get near-real-time alerts regarding even small deviations from the protocol, communicate with the patient and resolve issues in real-time. For patients at home, fast detection and response enable the clinical operations team to achieve extremely high protocol compliance.

Patient compliance automation for clinical trials - shaking hands

Chronic diseases

Chronic disease studies are conducted in real-world conditions with the patient at home. With AI-based detection and response and adaptive reinforcement of patient adherence, the CxO team can confidently complete studies and submission milestones on time and under budget.

Overview

Real time data feed

Data from investigators (EDC), patients (ePRO) and wearables (Flask API)

Patient compliance automation

Immediate picture of protocol compliance across sites, patients, cohorts

Cloud based

No need for IT. Just use it.

Your control

Your own measures, your own real-time alerts your own visual analytics of compliance trends.

Unlimited usage subscription

Unlimited users, data, sites, analytics.

Don't run your clinical trial

Run it smart.

  • 1Build a robust clinical trial data model
  • 2 Discipline equals speed
  • 3Pay attention to your date and time fields
  • 4Prioritise deviations.
  • 5Assess risk and prepare for change
  • 6Do not DIY your EDC
  • 7How to run clinical trials fast
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