Accurate. Timely. Insightful
Gain insights into device performance and efficacy with the collection of real-world evidence across the care continuum. Patient data can now be presented in a specific way that can help clinicians personalise care.
A platform that scales with your market requirements
Our EU MDR Class IIb regulated platform is the most flexible health data collection platform of its kind, and can scale with your market requirements. With support for more than 60 countries and 10 languages, we enable near real-time, real-world data collection and can deliver RWE in your operating markets worldwide.
Quality insights at an individual and population level
Huma’s platform provides access to aggregated data in one convenient dashboard, including digital data and ePRO. Connected devices capture a range of biomarkers in near real time, ensuring objective data collection with higher accuracy and minimal human error, while data visualisation and overlay tools give clinicians easier ways to uncover patient insights at an individual and population level.
Increase productivity. Reduce backlogs.
Our flexible, modular design allows you to manage multiple therapeutic area waiting lists with a single platform solution and secure additional outsourced clinician resources for face-to-face, virtual, and remote care. Huma enables multiple teams and specialists to review patient data and clinician notes on a unified dashboard for improved clinician collaboration.
Regulatory, safety and compliance
MHRA registered Medical Device Class IIb
US Food and Drug Administration Medical Device 510k # K230214
ISO 13485: 2016 certified (Medical Devices: Quality Management Systems)
ISO 27001: 2013 certified
Committed to GDPR compliance
NHS Registration on Data Security and Protection Toolkit
CyberEssentials / CyberEssentials Plus