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Funders increasingly expect confidence in data quality, auditability and project management before money is committed. PeopleWith gives you that from the start, so the only question left is whether your research is worth answering.
Data with a full provenance chain
Layer electronic health records with data direct from patients: symptoms, PROMs, PREMs and quality of life, alongside biomarkers, wearables and home devices. Every entry carries automated metadata from source to evidence output.
Everyone your project touches, in one place
Guide research and clinical teams across multiple sites through their work commitments, and invite patients and carers to take part through seamless digital recruitment and consent, proven to lift recruitment and retention.
Governance built in, not bolted on
A governance roadmap signposts the exact pathway for each project type, and governance professionals review every project before go-live. Simple or complex, requirements are met without slowing delivery.
1
Set up and activate sites
Follow the governance pathway for your project type and track every work package, from site engagement to full activation.
2
Recruit and consent patients
Surface eligible patients, including through our EMIS collaboration reaching more than 17 million UK primary care patients across 2,000+ practices, with digital eConsent.
3
Capture data and report
Collect clinical and patient-reported data, then share near-real-time reporting through role-specific dashboards, with access granted on a permission basis.
Clinical teams see what has been captured for each participant, who entered each value and when. Metadata records every interaction on the platform, so clinical-grade data is presented with provenance.
Clinical dashboard, patient registry view. Identifiers blurred.
Academic and public health research
Heads of department in faculties of medicine use PeopleWith to strengthen grant applications, then deliver funded work on time with data provenance built in throughout.
Pharmaceutical companies and CROs
Reduce the time and cost of delivery, and move from aggregated population data to patient-level, longitudinal UK evidence aligned to NHS, MHRA and NICE standards.
Health societies and charities
Access individualised, multimodal data for deeper insight into health conditions, and build patient registries that inform future research.
Academic research trials with the University of Oxford and Imperial College London.
Live, funded patient registries anchored by a Society for Endocrinology partnership.
An NHS Trust collaboration with Royal Brompton & Harefield.
Patient support, real-world evidence and patient experience projects commissioned by life-science companies.
1,400
patients recruited within 5 weeks of approval
9,000
patients recruited and retained within 7 months
<1%
participant attrition
45%
lower recruitment cost than traditional methods
See how PeopleWith manages data, people and governance for your next study, from approval through to completion.
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