Hersteller

Digitale Begleiter für Medikamente und Medizinprodukte.

Unsere digitale Gesundheitsplattform ermöglicht es Ihnen, personalisierte digitale Begleitlösungen zu erstellen, die die Wirksamkeit unterstützen können und die Zugänglichkeit von Daten verbessern.

Let's talk

myoncare für Hersteller

Analoge Produkte digital erweitern.

Entwickeln Sie digitale Therapie- und Produktbegleiter, um Ärzte und Patienten von der Vorsorgeuntersuchung und Diagnose bis hin zur langfristigen Therapieunterstützung zu begleiten.

Symptom-Monitoring in Echtzeit

Nahtlose Patientenbetreuung mit Echtzeitüberwachung der Symptome und Förderung der Therapietreue durch Erinnerungen und Aufklärungsinhalte.

Aufbau intersektoraler Netzwerke

Integrating all stakeholders around the patient - so the right action happens at the right time

Anonymisierte Real-World-Daten für Studien & Post-Market-Surveillance.

Benefit from a comprehensive compliance network to ensure adherence to regulators.

Anwendungsfälle für Pharma und Medizintechnik

Transformieren Sie Versorgung und Evidenzgenerierung mit einer Plattform

Befähigen Sie Ärzte und Patienten zu einer strukturierten Begleitung der gesamten Patientenreise, gewinnen Sie anonymisierte Real-World-Daten für Studien und Post-Market-Surveillance und automatisieren Sie Ihre Studienprozesse – alles in einem datengetriebenen Ökosystem.

Krankheitsmanagement

Empower patients to stay healthy - supported by insurers and employers who value proactive care.

Therapie-begleiter

Reduce complications, shorten hospital stays, and enable seamless recovery with remote monitoring and communication.

Real-World Evidence

Reduce complications, shorten hospital stays, and enable seamless recovery with remote monitoring and communication.

Begleiter für klinische Studien

Verwalten Sie Studienteilnehmer, ePROs und Besuchstermine digital, um die Compliance und Datenintegrität über alle Standorte hinweg sicherzustellen.

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Trusted By

myoncare platform

Patient-centered communication
& automation of care.

One platform connecting patients, care teams, and data. myoncare automates risk assessments, health monitoring, reminders, education, and telecommunication - all in one compliant infrastructure.

We’ve invested over 800,000 hours

to get the tech, compliance, and infrastructure right
– so you don’t have to.

Create medical
content in no time

with our ai-powered content management system & pathway builder.

100+ features combined in one platform.

Choose from numerous modules to create customized solutions:​

Regulatory-ready
& easy to integrate.

Designed to meet the highest standards for compliance, interoperability, flexibility, and research-driven collaboration.

Certifications

Qualität & Sicherheit by Design.

MDR Class IIa​

myoncare is certified under the MDR​

The platform myoncare is certified according to MDR (Regulation (EU) 2017/745 on medical devices) for Class IIa medical devices.​
ISO 13485: 2016​

Quality Management for Medical Devices​

This internationally agreed standard sets out the requirements for a quality management system specific to the medical devices industry. ​
ISO/IEC 27001: 2022​

Information Security Management System​

The information security management of ONCARE is based on the ISO 27001 principles and ensures the security of information assets whether in-house or entrusted to us by our customers.​
FDA Approval​

myoncare is approved in the US according to FDA​

The healthcare platform myoncare is approved in the US in accordance with FDA standards. ​
GDPR Conformity​

IITR Certified Data Protection​

Our data protection complies with the privacy requirements of the EU GDPR and DSGVO, confirmed and certified by the Institute for IT Law (IITR). ​
ISO 14971​

Application of Risk Management to Medical Devices​

The standard describes the processes for identifying the hazards associated with the medical device, to estimate and evaluate the associated risks, to control these risks, and to monitor the effectiveness of the controls.​
IEC 62304​

Medical Device Software Lifecycle Processes​

The quality management system of ONCARE  implements IEC 62304 as a framework throughout the software life cycle processes.​
IEC 82304​

Health Software Product Safety​

The standard applies to the safety and security of stand-alone health software products and points to ISO 14971 and IEC 62304 for risk and SW lifecycle processes.​
IEC 62366​

Medical Device Usability​

Relevant parts of the standard are used during risk management activities and UI/UX design.​
The standards and certifications mentioned here refer to the QMS and ISMS of ONCARE GmbH. ONCARE is responsible for the development of the myoncare healthcare platform. 
FAQ​

Wir beantworten Ihre Fragen
zu myoncare.

Was ist myoncare?

Wie kann myoncare mir helfen?

In welchen Bereichen kann myoncare zum Einsatz kommen?  

Wie funktioniert das Content Management System?  

Ich habe keine Zeit selbst Inhalte zu erstellen, gibt es hierfür eine Lösung?

Was bedeutet Medizinprodukt der Klasse IIa? Welche Vorteile hat dies?

Welche technischen Anforderungen gibt es?