Associations

From guidelines to real-world care

You define what good care looks like in your specialty. myoncare turns that definition into a digital care pathway your members activate and whose effect you can measure.

Let's talk
What myoncare does for you

You develop standards — with myoncare, you translate them into scalable, digital care pathways, connect members, and make care outcomes measurable.

myoncare is an FDA-listed platform made up of a web application for care teams and an app for patients. Your association builds the care pathways in the content management system, approves them, and evaluates the patient journeys that result.

Der Care Pathway Builder im Careplan Manager: ein Assessment verzweigt je nach Ergebnis in drei unterschiedliche Monitoring-Fragebögen.

Level 01

Your association

Your standard reaches every member at once, and your care pathways are adopted by members directly.

Level 02

Your members

Sie gewinnen ein Werkzeug, das entlastet und Therapietreue fördert, ohne ihr Praxis- oder Klinikinformationssystem zu wechseln.

Level 03

Their patients

They stay supported continuously between appointments. Every answer becomes a data point your association can evaluate.

FDA-Iisted platform Hosted in the US No IT project required
How it works

Build, roll out, evaluate

Three steps that take your standard from published to genuinely applied — and measurable.
01 · Build

Your guideline is applied consistently

You turn your guidelines into pathways the platform runs, clinical content unchanged. Today each practice interprets it its own way; once live, all follow the same steps. Your committee releases every pathway.

Prävention und Früherkennung mit myoncare
02 · Roll-out

IYour members come on board, without switching systems

Member practices and hospitals activate the pathway and work from the same basis, with defined access rights. The existing EHR carries on unchanged. myoncare sits alongside it, not in its place.

Digitale Begleitung vor und nach einem Eingriff
03 · Feedback loop

For the first time you seewhat happens across the field

PROMs, scores, events and patient journeys are captured structured during routine care, not as extra documentation. They form the basis for registries (including CMS Qualified Clinical Data Registries, or QCDRs, for MIPS reporting), quality reports and your advocacy work.

Begleitung bei chronischen Krankheiten mit myoncare
Your benefits

What your association gains as an organization

A guideline that runs as a live pathway does more than standardize care. It gives your association reach, evidence and leverage.

Your standard takes hold

What your committee decides is applied the same way by every connected practice and hospital, and the outcome data comes back to you. Your clinical work becomes a demonstrable contribution to quality of care.

Membership becomes tangible

You give members something that lightens the load in everyday practice. The membership fee gains a return you can show, and name when recruiting.

You argue with figures, not assumptions

Conversations with payers and CMS, advocacy and grant applications rest on outcome data from your own specialty, not on literature and isolated observations.

You take on no technology risk

The platform is FDA-listed, audited regularly and hosted in the US. Your content and data can be exported at any time, so nothing locks you in.

Use cases

Where associations typically start

Whether you want to spread standards across the field, evidence quality, strengthen continuing education or set up projects with third parties: each of these four routes can start on its own and be connected later.

Arztpraxen und Kliniken
One standard pathway per indication

You approve a pathway, your member centers activate it. No on-site configuration. The most common entry point, because one indication is enough.

Medical Creator
A registry that builds itself

Data is created where treatment happens. Members record nothing extra, and you get an analysis that would otherwise need its own budget.

Patienten
Continuing education on real patient journeys

Your CME courses work with what actually happens in practices, not constructed cases. That sharpens the content and shows where recommendations get stuck.

Versicherungen
Joint projects with hospitals and industry

Working with hospitals, industry or payers needs something to show. A running program is that proof, and it extends to further regions.

Trusted by hospitals, payers and partners

Frequently asked questions

Answers to your questionsabout myoncare

myoncare is an FDA-listed health platform consisting of a backend for care teams and a smartphone or web app for patients. Digital content can be created in the backend and then sent to patients in the smartphone app. From their dashboard, care teams can manage their patients, filter them by a range of criteria, track their health and communicate with them directly, by video call or chat.

myoncare is an FDA-listed health platform consisting of a backend for care teams and a smartphone or web app for patients. Digital content can be created in the backend and then sent to patients in the smartphone app. From their dashboard, care teams can manage their patients, filter them by a range of criteria, track their health and communicate with them directly, by video call or chat.

Patients are enrolled at the point of care by QR code. Sites and satellites mirror how care actually happens: a hospital department can lead the care pathway, while external clinicians join as satellites and see only the patients assigned to them or whose QR code they have scanned. The backend is built to be operated by clinical users without programming knowledge, and connects via HL7 for patient and diagnosis data from the EHR, FHIR for exchange with external health systems, and LOINC-conformant mapping for wearable data. That way sites do not have to re-enter what they already hold.

Not necessarily. The content management system (CMS) is the heart of myoncare: content can be created, given automation rules and combined into care pathways. The interface is deliberately designed so that it can also be operated by users without programming knowledge. If you do not have the time or the inclination to create content yourself, our content team can support you in building your own content, and pathways you have built once can be reused as templates. Please get in touch for more information.

myoncare is listed with the U.S. Food and Drug Administration (FDA). The platform is developed by ONCARE GmbH under a quality management system certified to ISO 13485:2016 — the standard that FDA's Quality Management System Regulation (21 CFR Part 820, in effect since February 2, 2026) incorporates by reference — together with ISO 14971 for risk management and IEC 62304 for the software lifecycle, audited regularly by TÜV SÜD Product Service GmbH. Outside the US, myoncare is CE-marked as a Class IIa medical device under the EU MDR. For you, this means documented and audited development, risk management and post-market processes that your compliance and procurement teams can review. Building your program on a platform that already has this in place takes that work off your program.

myoncare is listed with the U.S. FDA. ONCARE GmbH, which develops the platform, holds ISO 13485:2016 (quality management for medical devices) and ISO/IEC 27001:2022 (information security management system) and applies ISO 14971, IEC 62304, IEC 82304 and IEC 62366. In the US, data is hosted on US servers.

Outside the US, myoncare is CE-marked as a Class IIa medical device under the EU MDR, and GDPR compliance for EU customers is confirmed by the Institute for IT Law (IITR).

The standards and certifications listed refer to the quality management system (QMS) and the information security management system (ISMS) of ONCARE GmbH, which is responsible for developing the myoncare health platform.

As of July 2024:
using myoncare requires Windows 10, macOS 11.11 or Ubuntu 20.0 (or higher), a stable internet connection of at least 10 Mbit/s with a maximum latency of 200 ms, and a current version of Chrome, Firefox or Safari. For use on a tablet you need at least iOS 13.0 or Android 11.0. Your patients need a smartphone with an internet connection and at least iOS 13.0 or Android 11.0.

Your instance is hosted on US servers operated by a provider validated by myoncare — with nothing for you to do.

To connect to existing clinical systems, myoncare supports the established healthcare standards: HL7 for patient and diagnosis data from your EHR, FHIR for exchange with external health systems, and LOINC-conformant mapping for wearable data. Setting up these interfaces involves additional effort and cost.

With myoncare you can easily create digital care pathways that give your patients additional support along their health journey. myoncare can help to improve compliance, identify risks and complications early, capture health data in structured form, reduce patient uncertainty and increase satisfaction. The dashboard keeps your patients clearly in view, lets you filter them by various criteria and interact with them directly by chat, video call or data transfer.

myoncare can support doctors and patients across all indications. The only exception are conditions that make using a smartphone impossible, e.g., diseases of the central nervous system. Digital content can also be created to support patients in taking medication or using medical devices, or to provide health plan members or employees with preventive content, for example. The range of possibilities is very broad.

The content management system is the heart of myoncare. It lets you create content easily, attach automation rules to it and combine it into care pathways. The CMS interface was deliberately designed to be intuitive, so that users without programming knowledge can operate it easily too.

If you do not have the time or the inclination to create content yourself, our content team can support you in building your own content, and pathways you have built once can be reused as templates. Please get in touch for more information.

myoncare is listed with the U.S. Food and Drug Administration (FDA). The platform is developed by ONCARE GmbH under a quality management system certified to ISO 13485:2016 — the standard that FDA’s Quality Management System Regulation (21 CFR Part 820, in effect since February 2, 2026) incorporates by reference — together with ISO 14971 for risk management and IEC 62304 for the software lifecycle, audited regularly by TÜV SÜD Product Service GmbH. Outside the US, myoncare is CE-marked as a Class IIa medical device under the EU MDR. For you, this means documented and audited development, risk management and post-market processes that your compliance and procurement teams can review.

As of July 2024:
Using myoncare requires Windows 10 (or later), macOS 11.11 (or later) or Ubuntu 20.0 (or later), a stable internet connection of at least 10 Mbit/s with a maximum latency of 200 ms, and the latest version of the Chrome, Firefox or Safari browser. For use on a tablet you need at least iOS 13.0 or Android 11.0. Your instance is hosted on US servers operated by a provider validated by myoncare — with nothing for you to do. Your patients need a smartphone with an internet connection and at least iOS 13.0 or Android 11.0. Setting up interfaces to your EHR or other systems involves additional effort and cost.

Let’s talk about your association

In a confidential first conversation we work out which indication makes the best entry point, what a pilot could look like, and which questions your committee wants answered.

Let's talk