Europe's first consent-borne research environment.
People's Research is a consent-borne research platform for clinical researchers and project leads. Studies run on primary-care data from everyday practice. Every data point is granted actively per study. EHDS-aligned, GDPR-aligned, EU-hosted. Record data never leaves Europe.
Three studies we have seen
Three concrete examples of what researchers use us for. Stylised - but this is what a study looks like in practice.
A department wants to know whether a new treatment algorithm reduces blood-pressure complications over 24 months. We find 3,200 adults with type 2 diabetes across 14 general practice clinics. All have agreed to participate.
A hospital follows vaccine response in citizens over 75. The study runs three months. When a participant withdraws consent, they drop out of the analysis the same day.
A postoperative pain study collects patient-reported pain scores from wearables and questionnaires, linked with chart notes. The clinician sees their own participant group live.
Study flow
How a study runs with us. Same rhythm whether a department, a hospital or a university starts it.
You formulate what you want to investigate - which patient group, which treatment, which outcome. We help with the protocol if you want.
We show how many citizens match your inclusion. And how many of them have already said yes to research. You see the number before you commit.
Data from chart, wearables and citizen responses flows in continuously. You see the participant group live. If a participant withdraws, the dataset updates the same day.
You own the publication rights. Also if a pharma company has co-funded. It is written into our independence policy.
Have you been invited to take part in a study? See how it works from the participant's side
Four roles
Research with us does not interfere with clinical practice. The clinician charts as always, the research runs alongside, and the participant's consent is the only thing that opens data for the study. The citizen owns the data, the clinic holds the chart, the researcher sees the participant group - not individual citizens. People's keeps the trail of who has seen what.
Owns the data. Controls the consent. Can withdraw it whenever.
Holds the chart. Treats the patient. Has nothing new to learn.
Sees the participant group as a whole - not individual citizens.
Keeps the trail of who has seen what - and when.
We are in the design-partner phase. Researchers, clinical departments, universities and medtech companies - tell us what you are looking for, and we respond within two working days.
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