Clinical trial data management in the cloud.
Where simplicity meets speed meets security.
Where simplicity meets speed meets security.
At Flask Data, we define ourselves as a new kind of CRO. Our company is a digital CRO, with a technology-business orientation. We believe that speed of execution and high quality data is key to your success.
The Flask Data digital platform enables us to provide you with a highly cost-effective solution for real-time status of your clinical data.
The Flask Data platform includes single sign-on for sites, CTMS, EDC, ePRO, randomization, trial supply, and data management; scalable from 10 patients to 40,000. You can grow from early stage biotech pilots to Phase 1, Phase 2, Phase 2B, Phase 3, regulatory submissions, post-marketing studies and bioequivalence without changing systems.
We know that there is no single solution that works for every clinical trial.
We specialize in understanding your unique situation.
We bring years of technology, clinical trials, and business know-how to navigate you on the rocky road to
market, from your first patient to successful regulatory submissions.
The Flask Data Digital CRO platform enables us to provide you
with an affordable, tailor-made solution for your needs and for your budget.
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
One sign-in for all apps
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.
Digital CRO solutions – zero project overhead
Our mission is to make it radically simple to get the right clinical data management solution for the best price.
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.