When patient compliance to treatment counts

Whenever patient compliance is critical, our fast data platform helps you achieve high levels of patient compliance and submit faster to FDA.

Pre-submission clinical trials

Patient compliance assurance is often an FDA requirement for a regulatory study.

Patient compliance is critical to the success of clinical research of neurodegenerative diseases, cannabis, migraine, rheumatoid arthritis, asthma, diabetes, atopic dermatitis, chronic constipation, pain management and heart failure.   Assuring and reinforcing patient adherence over time is particularly acute in home use devices and drug treatments.

Flaskdata.io has patent-pending AI technology for monitoring and reinforcing patient compliance to the treatment protocol in regulatory clinical trials.

Our data monitoring engine enables us to develop specific compliance models from within our own labs to fit the needs of your clinical trial and enable you to achieve the highest levels of patient compliance and speed up your time to data analysis and regulatory submission.

Post-marketing research

The output of the patient compliance AI is an adherence strategy for your intervention based on your clinical evidence. This becomes the basis for a companion mobile app, private-branded for your intervention to help sustain high levels of patient adherence in real-life clinical practice.


100X faster to deviation detection in medical device studies.

Automated Patient compliance deviation detection and response on the flaskdata.io platform for a connected medical device clinical trial is 100X faster than manual monitoring. Automated compliance monitoring analytics and real-time alerts let you focus your site monitoring visits on work with the PI and site coordinators to take total ownership and have the right training and tools to meet their patient recruitment and patient compliance goals.