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epro application for clinical trials visualization

We specialise in patient-centric drug and/or device studies with emphasis on pain, gastro, diabetes and CNS helping sponsors achieve high levels of protocol compliance with low data latency using AI-driven detection and response.

We get up in the morning thinking about one thing – how to help you succeed faster in your clinical trial. We love challenges. is an Israeli technology company that provides Patient compliance automation for clinical trials. Automation eliminates non-value-added people and paper activities and  saves 90% of study monitoring and clinical data management costs.

The patient compliance automation platform is a complete solution for decentralised clinical trials, patient-centric interventions, digital therapeutics and site-less trials.The platform integrates EDC, mobile ePRO and connected devices using a continuous data feed.    The Detect & Respond sub-system processes the continuous data feed to provide an immediate picture of protocol compliance for your patient-centric research.

Automated playbooks provide adaptive reinforcement messages for patients in their own time and treatment frame and help them achieve high levels of adherence. cloud services are HIPAA and 21 CFR Part 11-compliant and give life sciences CxO teams a complete picture of their studies at a fraction of the cost and over 100X faster than current manual monitoring activities.

Create and monitor measures of GCP compliance

You can create and remotely monitor measures of GCP compliance and site performance from all the data sources in your study: EDC,  ePRO, mobile API and medical devices used by subjects.    You can create alerts on measures over threshold and visualize compliance trends over time.

Monitor and reinforce patient compliance for any sized study.

Patient compliance is not only part of GCP, it is crucial to sustaining the statistical power in your study since non-compliant patients need to be dropped and replacements need to be recruited costing time and money, delaying completion of the study and placing study at risk.

FlaskData alerts and  visual analytics help you zoom in to patients and micro-manage ePRO and treatment compliance to resolution.

You can do this in a Phase I study with 20 patients in a global multi-center clinical trial with  thousands of patients.   FlaskData is an easy-to-use cloud service in a pricing model that enables you to start small and grow and pay for the features you need.

Unchain your brain from time-consuming paper and data extracts

Is complex data a challenge to your brain and your pocketbook? This is what we do – at the beginning we’ll help guide you to the right data model for your study. Align your CRF and your protocol. Get rid of the black holes. Deliver highly effective real-time remote monitoring that let’s you focus on managing the study instead of running data extracts and building more and more Excels.

Work hard. Sleep well.

We started this company after spending years in the trenches of cyber security for telcos and medical device companies. FlaskData technology runs on high performance, secure cloud instances and integrates with EDC and PRO and the Flask mobile/device API service. Your clinical trial data is stored in secure cloud instances. Protected by strong access control and extended SSL transmission security and a team dedicated to data security.

Dig us.

We’re into fanatic support.

FlaskData is more than technology. It’s about people – listening to you and helping you achieve speed to results in your study by eliminating avoidable rework.


Discover superior value

FlaskData includes the beautiful Flaskdata CTMS, ePRO, eSource and FlaskData API that enables you to easily integrate connected medical devices into your study.

Flat-rate, unlimited usage (unlimited users and data) subscriptions enable you to focus on your research and grow without worrying about additional license fees.