Today clinical trials are monitored by hand. This is a slow, expensive and yet must-have process in order to comply with GCP.
Manual monitoring currently takes 5-12 weeks to log deviations and costs 25-30% of the total study budget.
Flaskdata is a digital platform for patient compliance automation for clinical trials. You get 3 in 1:
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.
Patient compliance assurance is often an FDA requirement for a regulatory study and not just a critical scientific requirement.
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.
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.