Quickly and efficiently create a study for a specific therapeutic area
Our platform is not hard coded, which makes it easier to create a study for your specific therapeutic area quickly and efficiently , and collect high-quality data specific to your TA protocol.
Our highly configurable platform—combined with deep domain expertise—enables you to deploy a robust clinical trial that’s specific to your therapeutic area. Continuous device data collection ensures higher accuracy.
Powerful, modular SDK (Software Development Kit) that can adapt to your exact TA protocol
With a platform that can be, without hard coding, reconfigured in minutes, we help ensure your study’s protocol integrity. Our out-of-the box option, is a pre-configured setup for major therapeutic areas which delivers faster TA study deployment.
Build a therapeutic set-up for your precise TA needs
Huma’s easy-to-configure end to end solution, without hard coding, allows a faster setup for your specific study requirements. Our platform can also be customised for specific projects where integration with an EDC is required.
Huma’s platform features pre-built modules including eConsent, ePRO and eCOA that can be configured and adapted to your specific protocol, enabling quick setup of your therapeutic study requirements. This includes our unique approach to questionnaire branching which can save valuable time in setup and study changes.
Regulatory, safety and compliance
MHRA registered Medical Device Class IIb
Part 820 ff
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