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The patient voice, actually heard.

Structured insight from patients and advocates - the people with lived experience. The asynchronous format removes the burden of attendance and lets quieter voices contribute fully.

Book a demoSame platform, same guarantee. Only the scenario changes.
The problem

Why patient panels under-deliver

  • Travel and fixed meeting times are a real burden for people managing a condition - so panels skew to whoever can attend.
  • In a live room with clinicians and company staff, the patient voice is the easiest one to lose. The risk isn’t low turnout - it’s tokenism.
  • What patients do say rarely survives as more than meeting notes - unattributed and unusable when program decisions are made.
How Rumi runs it

One platform. This scenario.

  1. A safe, welcoming venue

    Patients contribute from home, on any device, with no travel and no video-call pressure - and time to say things properly.

  2. Fair share of voice by design

    Structured topics and active moderation draw in quieter panellists; clinical and company voices can’t dominate.

  3. A record you can act on

    Plain-language questions, reviewed at each patient’s pace - and a structured, attributed record of the patient voice at the end.

Why Rumi wins here

Fairness where it matters most

A fair share of voice matters most where the power imbalance is greatest. Rumi designs it in rather than hoping for it.

Consent and privacy answered

Dedicated invite-only rooms, strict data walls and an auditable record - a compliance posture built for sensitive communities.

Participation without burden

No travel, no fixed slot, any device - and the 100% participation guarantee applies to patient panels exactly as it does to advisory boards.

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The insights generated from this hugely successful patient panel will inform the scoping and design of future patient support initiatives. We feel we are one step closer to the patient voice.

Rare-disease patient advisory boardPatient Engagement Lead - Sobi
The guarantee travels

100% participation is as binding here as on an advisory board.

Same monitoring, same moderator tools, same written terms: a defined panel, a defined bar for participation, and a remedy if we miss.

Patient advisory panels: your questions

What is a patient advisory board platform?

A patient advisory board platform runs structured engagement with patients and advocates online. On Rumi the panel runs asynchronously in a safe, moderated, invite-only room: patients contribute from home at their own pace, moderation keeps the share of voice fair, and the output is a structured, attributed record of the patient voice.

How does Rumi reduce the burden on patient panellists?

No travel, no fixed meeting time, and nothing to install - patients contribute from any device, in their own time, across an extended window. That convenience is what makes full participation possible for people managing a condition.

Is Rumi appropriate for sensitive patient communities?

Yes. Every panel runs in its own dedicated, invite-only room with a complete auditable record, data strictly walled per engagement, and consent handled up front. Moderators - often a patient-advocacy lead - keep the conversation safe and two-way.

See every voice heard, in full, on your own use case.

Book a demo
Thirty minutes with Steve Royle, founder, on your use case.