FDA-listed
Registered and listed with the U.S. Food and Drug Administration. In the EU, myoncare is CE-marked as a Class IIa medical device under the MDR (Regulation 2017/745).
Together we are shaping the future of healthcare. We are building a certified care platform that takes pressure off care teams, involves patients and measurably improves the quality of care.
FDA-listed
Preparation before admission
Follow-up after discharge
Integrates with your EHR
With myoncare we are rethinking health management and care delivery: a digital ecosystem that connects everyone involved in healthcare and makes real-world data accessible.
One app for patients: Patients receive their care pathway, tasks, reminders and educational content on their own smartphone. Readings and symptoms are captured where they occur — in everyday life, not at the next appointment.
One dashboard for the care team: Every patient at a glance, filterable by the parameters that matter for your indication. Abnormal values are immediately visible, and chat and video consultations run through a telemedicine module certified by the KBV, Germany’s National Association of Statutory Health Insurance Physicians.


A certified medical device comes with audit reports, standards and documentation. We provide them during procurement instead of submitting them afterwards.
Registered and listed with the U.S. Food and Drug Administration. In the EU, myoncare is CE-marked as a Class IIa medical device under the MDR (Regulation 2017/745).
TÜV SÜD Product Service GmbH audits our quality and information security management regularly. The audit reports can be provided during procurement.
US customer data is hosted on servers in the US, with encrypted transmission, role-based access and traceable activity designed to support your HIPAA obligations. For EU customers: GDPR compliance confirmed by the Institute for IT Law (IITR) and BSI C5 attestation (international).
Information security and quality management to the standards your own review will reference. Plus ISO 14971 for risk management and IEC 62304 and IEC 82304. ISO 13485 is the standard FDA’s QMSR incorporates by reference.
Trusted by
Between discharge and follow-up, between the practice and the hospital, between what was prescribed and what actually happens in a patient’s daily life. Quality of care is lost in exactly those gaps — and that is exactly where we work.
They are not just in the brand book. They decide how we build products, who we work with and how we handle your data.
We do not believe in a one-size-fits-all solution, because we know reality does not work that way. We adapt easily to changing conditions by offering modular, scalable solutions for a complex and constantly changing ecosystem.
We are committed to creating a safe and solid environment for digital health, and we set the benchmark in data security. Because for people to trust technology, the solutions have to be dependable.
We are changing healthcare for the benefit of people. By putting patients at the centre of everything we do, we hold on to the most complete and sustainable view of care possible.
We focus on our strengths and build on synergies. Because we know that connected solutions lead to simpler, better care — and that is something we can only achieve together.
myoncare was founded on the conviction that modern patient care is more than a digital tool: it is an integrated experience that takes pressure off care teams, involves patients and measurably improves clinical quality.
Since then we have worked continuously on the same platform — not on a succession of products.
Medicine, regulatory affairs, engineering and customer support all work together in house.
DACH, the US and MENA. The same platform, adapted to each region’s regulatory requirements.
Therapies, medicines and medical devices can deliver better results when we bring patients on board as managers of their own health. Improved adherence and early detection of possible complications can be the key to better outcomes in many therapies.
In a first call we work out where myoncare fits in your organisation, who your dedicated contact will be and which documents your procurement team needs from us.
Let's talk