.png)
Enroll patients faster and keep them engaged longer for better clinical trial outcomes
Award-winning human-centered design and 25 years of experience understanding complex patient and client needs across 1400 deployments has given us the knowledge to optimise and impact each touchpoint across clinical trial phases.
From screening to eConsent to onboarding and ongoing patient monitoring, our streamlined user journeys have helped clients around the world accelerate time to “first patient in” and engage and retain participants through the study and beyond with minimal dropout.
Powering digital-first clinical research
eConsent
eCOA/ePRO
Telemedecine
Connected devices
Keep your trial participants engaged with multiple touch points
Daily check-in support, application alerts and notifications, site-to-participant messaging and Televisits enable seamless communication and deliver higher participant engagement.
Award winning, intuitive design encourages data entry and usage
Based on more than a decade of experience working directly with patients, Huma’s platform is easy to use and quick to deploy. We boast 90-95% patient adherence and retention rates1 across our deployments, and are a proud recipient of the prestigious 2022 Prix Galien award for digital health, widely regarded as 'pharma's Nobel prize'.
Our easy-to-use patient dashboard gives researchers direct access to key metrics and meaningful health indicators. While our ergonomic screen layout allows for quick and easy ePRO data entry.
Designed with flexibility in mind, you can extend trial participation rates by easily adding caregivers to assist with data entry on behalf of the participant (eg: for pediatrics, and other trials where participants may find it difficult to enter data manually).
Build participant confidence with the ‘Learn’ module
Huma’s ‘Learn’ module, easily accessible from the Huma app, helps your participants understand what to expect from your trial, with explainer videos, FAQs, disease education, dietary guidance and more as standard.
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
Save time and set-up costs with self-serve and fully-managed options
Our fully-regulated platform can be deployed across multiple countries and offers reliability and a high degree of user acceptance at scale.
Our powerful, modular platform includes pre-built components including eConsent, ePRO and eCOA that can be configured and adapted to your specific protocol and are ready to deploy on any cloud, saving time and reducing costs.
