Patient compliance
for clinical trials
  • You save 90% of your traditional study monitoring costs with automation.
  • As a result of using automation, you can detect and resolve non-compliance issues in hours instead of weeks.
  • Clinicians, patients and connected medical devices send data to the clinical data management platform.
  • Our code computes clinical measures and automatically checks for deviations.
  • You get alerts and your patients get reinforcement in real-time.
  • Your data is protected with strong security and privacy controls that comply with HIPAA, GDPR and 21 CFR Part 11.
  • Your budget is protected with friendly, fixed-price, unlimited usage subscriptions.
  • And one more thing - the compliance models you develop in your clinical trials can be reused to reinforce patient adherence in real life.


Patient compliance automation for clinical trials

For sponsors

Use the open Flask Data API to collect data from devices, wearables or mobile medical apps. Respond in minutes to deviations.

Patient compliance automation for clinical trials

For patients

Smart patient reminders to reinforce compliance without alarm fatigue and fixed tailoring.

Patient compliance automation for clinical trials - shaking hands

For business.

FlaskData accelerates time to submission by assuring high levels of patient compliance and fast acquisition of high quality data from sites, subjects and connected devices.


Real time

Access all the data, anytime, from anywhere.

Monitoring as a Service

Assure patient compliance and oversee your sites. Eliminate SDV with smart technology.

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 data subscriptions

As much as you need.

Don't run your clinical trial

Run it smart.

Straight-talk and a 6 step program to clinical trial success for entrepreneurs.
  • 1Don't make big CRO mistakes
  • 2Dispel study monitoring FUD
  • 3Secure your clinical data and IP
  • 4Reduce your time to submission
  • 5Reduce your total clinical trial cost
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