SOFTWARE AS A MEDICAL DEVICE

Drive innovation faster

Increase revenue opportunities and build better, differentiated products with remote patient monitoring and real-world evidence gathered across the care continuum.

Huma's EU MDR Class IIb approved and Class II FDA 510(k) cleared platform helps MedTech deliver on the promise of innovation through added value services, RWE collection and improved research support. Build stronger relationships with patients and customers while collecting insights to support the next phase of product development.

Increase patient and clinician engagement

Huma’s award-winning, patient-centric design improves clinician and patient engagement and outcomes, helping MedTech build stronger, longer-term relationships with care providers and customers. We have the potential to help clinicians by providing advice and recommendations for individual patients throughout their care journey.

We have a 90–95% adherence and retention rate1 across our care and research deployments as a result of our high engagement rates.

Huma clinician app screenshot.
Huma clinician app screenshot.
Huma clinician app screenshot.
Huma clinician app screenshot.

Increase patient and clinician engagement

Huma’s award-winning, patient-centric design improves clinician and patient engagement and outcomes, helping MedTech build stronger, longer-term relationships with care providers and customers. We have the potential to help clinicians by providing advice and recommendations for individual patients throughout their care journey.

We have a 90–95% adherence and retention rate1 across our care and research deployments as a result of our high engagement rates.

Explore novel reimbursement opportunities

Extending patient monitoring and engagement into pre- and post-operative recovery opens up new opportunities for MedTech reimbursement.

The Huma platform can collect and provide actionable insights for a wider patient population due to its Class IIb certification.

Regulatory, safety and compliance

CE 0297 icon.
EU MDR 2017/745 Class IIb certified

MHRA registered Medical Device Class IIb

US FDA icon.
21CFR820 US FDA Class II

US Food and Drug Administration Medical Device 510k # K230214

ISO icon.
ISO certifications

ISO 13485: 2016 certified (Medical Devices: Quality Management Systems)

ISO 27001: 2013 certified

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Data protection / infosec

Committed to GDPR compliance

NHS Registration on Data Security and Protection Toolkit

CyberEssentials / CyberEssentials Plus

Optimise surgical waitlist management

Huma’s platform optimises surgical waitlists via pre- and post-surgical monitoring with proactive identification of patient deterioration. Smart alerts and individual patient  thresholding and targeting ensure personalised care while maximising population health management.

Huma’s “Learn” module helps patients build understanding, confidence, and reassurance about their condition and ongoing plan of care, and is proven to support higher medication adherence.2

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Sources

1

Range of data from across a number of Huma projects

2

Sarraju, A., Seninger, C., Parameswaran, V. et al. Pandemic-proof recruitment and engagement in a fully decentralized trial in atrial fibrillation patients (DeTAP). npj Digit. Med. 5, 80 (2022). https://doi.org/10.1038/s41746-022-00622-9

https://www.nature.com/articles/s41746-022-00622-9