Climedo provides an eCOA system for clinical data collection, including EDC, eCRF, ePRO, and eSurveys. Their platform enables flexible, patient-centric data capture that increases compliance and data quality. This digital approach saves time and costs in clinical studies and surveys through automation and remote monitoring capabilities.
Funding
$7.1M raised to dateRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Product
Problem
Traditional methods of clinical data collection, particularly in non-interventional studies and real-world data (RWD) collection, often rely on paper-based processes, leading to increased time, costs, and potential errors in data management. The lack of patient-centric and flexible data collection tools can also result in lower patient compliance and reduced data quality.
Solution
Climedo offers a web-based eClinical platform designed to streamline the collection of high-quality clinical data through electronic Clinical Outcome Assessments (eCOA), electronic Patient-Reported Outcomes (ePRO), and RWD. The platform provides solutions such as Electronic Data Capture (EDC), electronic Case Report Forms (eCRF), and electronic surveys (eSurveys) to enhance data quality, improve patient compliance, and reduce the time and costs associated with clinical research. By offering a patient-oriented and flexible data collection approach, Climedo enables faster study results, automated processes, and remote monitoring capabilities. The platform supports various study types, including Phase I-IV, interventional, non-interventional, and Real-World Evidence studies.
Target Audience
Climedo's primary customers include pharmaceutical and biotech companies, medical device manufacturers, Contract Research Organizations (CROs), hospitals, and research institutions involved in clinical studies and data collection.
Features
- EDC system for electronic data capture
- eCOA and ePRO for patient-reported outcomes
- eCRF for electronic case report forms
- eSurveys for conducting electronic surveys
- Real-time dashboards and visualizations for study progress monitoring
- eConsent capabilities for electronic informed consent
- Support for hybrid and decentralized clinical trials (DCT)
- Compliant with GDPR and other relevant data protection regulations
- Role-based access control
- Automated reminders to increase patient compliance