Europe's first consent-borne research environment.

How a study runs with us.

We help clinical researchers and project leads run studies on data from everyday clinical practice - with full consent and without the participant's record data leaving Europe.

Three studies we have seen

What you can investigate in clinical practice.

Three concrete examples of what researchers use us for. Stylised - but this is what a study actually looks like.

Diabetology

Type 2 diabetes in general 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.

3,200 participants · 24 months

Vaccinology

Vaccine follow-up in older citizens

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.

1,450 participants · 3 months

Postoperative pain

Pain after surgery

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.

820 participants · 6 months

Study flow

Four steps - from question to answer.

How a study runs with us. Same rhythm whether a department, a hospital or a university starts it.

  1. 01

    Define your question

    You formulate what you want to investigate - which patient group, which treatment, which outcome. We help with the protocol if you want.

  2. 02

    Assemble the participant group

    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.

  3. 03

    Follow the participants

    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.

  4. 04

    Publish your findings

    You own the publication rights. Also if a pharma company has co-funded. It is written into our independence policy.

Coexistence

You are still the same department.

Research with us does not interfere with your clinical practice. The clinician charts as always. Only the participant's consent opens the data for the study - and the citizen controls this via their Wallet. No extra system for the clinician.

  • The clinician works in their own chart system as always
  • Researcher access is governed by participant consent, not by clinic IT
  • Citizen record data never leaves Europe
The clinic Care as always The research Runs alongside Consent

The participant's journey

From invitation to withdrawal.

You are never in doubt about what happens. Consent is per study, can be tailored per data type, and can be withdrawn with one tap. Also five years later.

  1. 01

    You receive the invitation

    The clinic or your People's Wallet sends a message: a study is looking for participants like you.

  2. 02

    You read what the study wants

    In Wallet you see the purpose, which data is used, how long the study runs, and who is behind it.

  3. 03

    You say yes, no, or tailor

    You can accept all, say no thanks, or opt out of individual data types. Your choice applies only to the one study.

  4. 04

    Your data flows in

    For the agreed period your chart notes, lab results or wearable readings contribute to the study - never identifiable to the researcher.

  5. 05

    You can withdraw the yes

    Whenever you want. One tap in Wallet, and your data is removed from future analysis the same day.

Responsibility

Nobody owns everything - and that is the point.

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. Four roles, four cards, no commingling.

The citizen

Owns the data. Controls the consent. Can withdraw it whenever.

The clinic

Holds the chart. Treats the patient. Has nothing new to learn.

The researcher

Sees the participant group as a whole - not individual citizens.

People's

Keeps the trail of who has seen what - and when.

  • 3.2k Participants who said yes Design-partner phase
  • 14 Clinics we collaborate with General practice + specialties
  • 100% EU-hosted Never on US cloud
  • Always Every participant can withdraw the yes Whenever. Also five years later.

Want to start a study?

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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