Faster submission
for medical devices
93% patient compliance in your next medical device study.

  • Flaskdata provides fast data acquisition from investigators, devices and patients
  • Automated deviation detection and response assures high levels of patient compliance to the protocol.
  • Reduces time to FDA submission by 6-12 months from pilot to pivotal study.
  • Strong data security and privacy controls. Flaskdata is HIPAA, GDPR and 21 CFR Part 11 compliant.
  • Consume Flaskdata on demand in transparent, fixed-price, unlimited usage subscriptions with guaranteed data portability.

benefits

Patient compliance automation for clinical trials

For medtech developers

Plug in the Flask Data API and collect data from medical devices, wearables or mobile medical apps. Respond in real-time 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 subjects and connected medical devices.

Overview

Real time

All the data, anytime, from anywhere.

Patient compliance automation

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.

  • 1Straight talk for medical device entrepreneurs
  • 2Why you cannot afford paper studies
  • 3Best-practices for implementing EDC
  • 4Security and privacy how-to
Click here to learn more