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Same day
clinical data and safety


Achieve same day data quality, patient safety and protocol compliance.

You need to comply with Good Clinical Practice (GCP);  the international ethical and scientific quality standard for the design, conduct, performance, monitoring, auditing, recording, analyses and reporting of clinical trials. delivers automated metrics in near-real-time for GCP compliance.  Metrics for protocol compliance, safety and data quality that you, your clinops team and sites can trust.

Rapidly bring studies to patients.
Using the no-code design app, you can build a study and go-live with patients in a week.  You can migrate from Rave and go-live on Flask in 3 weeks

Retain patients. Sustain adherence. 

Our platform is designed around a holistic trial process that is both human and data-centric. It is made to ensure that your patients and front-line site coordinators can successfully complete the trial. With a simple, intuitive UX and open access to data; your entire ecosystem of patients and clinical operations teams can take immediate decisions without frustrating, technology-top-heavy data management systems.

flaskdata collect, detect and act

Unleash unlimited possibilities for your product development with a cloud API

Flask cloud API unleashes unlimited possibilities for clinical developers. The entire Flask platform is exposed as a RESTful API. You can develop your own CTMS with less than 10 API calls.  You can collect data from devices and export data from the EDC into your own ML systems. Flask API can be integrated into any code that can call a RESTful API.   

Recruit patients and collect data anywhere you can connect the Flask API. Sites, mobile devices, digital therapeutics, patient-advocacy web sites, hospital systems, academic research organizations, pharmacies, community centers and of course – patients at home.

Tackle any challenge in your early stage drug and device projects

Early stage drug and device projects are often challenged by tight budgets and an inadequate Phase 1 protocol design. We provide you with robust digital data management tools that will enable you to work with a small head-count without compromising tight adherence to protocol requirements and careful monitoring of patient safety.

We provide creative, agile solutions for biopharma, connected drugs, connected medical devices, digital therapeutics and AI-driven medical applications that need to be validated for FDA approval.  We love challenges. We work with big, publicly-traded companies and 3 man medical device startups.  Thousands of patients around the world use the clinical data platform in the US, Israel, Europe, India and Brazil.

We will stand by you in good and bad times with fanatic service, straight-talk and the highest professional and ethical standards.

Designed for clinical trial data security and patient privacy

The online clinical data collection and automated monitoring applications and API services are designed and implemented using best practice software security and data privacy standards.  The system complies with HIPAA, CCPA, GDPR, 21 CFR Part 11 and Israeli Privacy Regulations.

HIPAA compliance
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