A world-leading platform for clinical trial data management.
EDC, Data management, Biostatistics.
Flask Data provides life science R&D teams with same-day clinical data and patient safety solutions. Flask Data Collect, Detect and Act unifies EDC with automated data and safety monitoring in the cloud for your clinical trials.
Our data management and safety monitoring solutions help you reduce risk to clinical data, patient safety, and protocol compliance.
Our mission is to promote clinical data observability as a core tool in the life science R&D industry. Better data, better science for patients.
Flask Data is a technology company specializing in clinical data management and monitoring.
We are accomplished at providing our customers with the most effective way to achieve high quality clinical data and assure patient safety. There is no single solution that works for every clinical trial. We work hard to understand your unique situation. We work with your team to develop the best solution to achieve high quality clinical data and assure patient safety, the same day you engage with patients and their devices.
Phase 1 clinical trials
Phase 2-3 clinical trials
Phase 4 and PMS
Food supplements
Cosmetics
Cannabis
Study management
Subject management
Population studies
Investigator studies
Study design
Medical IoT
Study management
Pre-screening
Remote data and safety monitoring
Protocol compliance automation
Data management tools
Pharmacovigilance
Connected devices
Digital therapeutics
Sports tech
Fem tech
Diagnostics
Design
Design and amend your eCRF with Flask Design – no-code visual forms designer and study build tool.
Collect
Collect data from code, humans and devices using EDC, ePRO, eCOA and the open Flask API.
Detect
Automate detection of issues with data quality, protocol compliance and patient safety.
Act
Automated alerts on clinical measures to reinforce protocol compliance and ensure patient safety.
The Flaskdata.io 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.
Same day data and safety solutions
Flask Data is on a mission to provide data observability for every clinical trial. Better data is better science for patients.
Copyright © 2022 Flask Data Ltd. All Rights Reserved.
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.
Flaskdata.io 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.
Using the Flaskdata.io 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
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.
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.
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 Flaskdata.io 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.