From prevention to aftercare: myoncare guides patients individually and without gaps. Care teams keep patient health in view at all times without having to review every single value, and are alerted precisely when risks are detected.
FDA-listed
Preparation before admission
Follow-up after discharge
Integrates with your EHR
Trusted by
Individual measures that strengthen health. Plus digital early detection that reveals risks before symptoms appear.
Digital guidance before and after the procedure, for less uncertainty, better preparation and faster recovery.
Seamless digital support in everyday life, for more confidence, better outcomes and a stronger physician-patient relationship.
Connect referrers, specialists, hospitals, laboratories and aftercare seamlessly and build virtual comprehensive care centers.
In just a few clicks you assign individual permissions for every participant and define who may view, document or release which data.
Whether hospital, practice, patient or payer: myoncare is the go-to tool for everyone who thinks about care digitally. No IT skills needed, ready in no time, on an MDR Class IIa platform.
Improve quality of care at lower costs
Build medical solutions in record time
Actively support your own health
Lower costs & strengthen patient safety
Increase the visibility of your products
Foster joint collaboration
Build care networks for entire regions & states
myoncare is FDA-listed, hosted in the US and operated by myoncare, Inc. in New York. The workflows your teams run in myoncare, from connected-device readings to care plans and follow-ups, support billable services such as Remote Patient Monitoring, Remote Therapeutic Monitoring and Chronic Care Management. And because the same platform meets regulatory requirements from the EU MDR to ANVISA, a program that works in one state can scale across sites and countries.
The platform meets the standards of the US Food and Drug Administration and is listed for the US market.
US customer data is hosted on servers in the US. Encryption, role-based access and traceable activity are designed to support your HIPAA obligations.
In the EU, the platform is certified as a Class IIa medical device under the Medical Device Regulation (EU) 2017/745.
This internationally recognized standard defines the requirements for a quality management system specifically for the medical device industry. It is also the standard FDA’s Quality Management System Regulation (21 CFR Part 820) incorporates by reference.
Information security at ONCARE is based on the principles of ISO 27001 and safeguards information assets, regardless of whether they are entrusted to us or to our customers.
The standard describes the procedures for identifying hazards associated with the medical device, estimating and evaluating the related risks, and monitoring the effectiveness of controls.
The ONCARE quality management system implements IEC 62304 as the framework for the entire software lifecycle process.
The standard applies to the safety of standalone health software products and refers to ISO 14971 and IEC 62304 for risk and software lifecycle processes.
Relevant parts of the standard are applied in risk management activities and UI/UX design.
The standards and certifications listed here relate to the quality management system (QMS) and the information security management system (ISMS) of ONCARE GmbH, which develops the myoncare health platform. myoncare, Inc. is the US company.
Whether a single practice, a hospital or an entire region: in a short call we show you exactly how myoncare works in your setting, with measurable outcomes instead of vague pilots.
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