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Digital boost for your medical devices

Unleash the full potential of your medical devices. The digital companion from myon.clinic supports patients during use with appropriate instructions, explanations, reminders and symptom queries.

One solution. Everything you need.

Our full-service offering for medical device manufacturers combines dedicated digital treatment paths with extensive features for management and interaction with patients.

Overview:

Short, automated screenings can be used to reach large user groups and raise awareness of disease risks and new medical products.

Benefits:

Interactive display achieves high engagement rates, users can be accompanied longitudinally, collection of anonymized data

Overview:

Ongoing patient support with real-time monitoring of complications and promotion of adherence through reminders, information and education.

Benefits:

Early detection of complications or risks, promotion of adherence, increased patient safety and satisfaction, possibility to collect anonymized data

Overview:

Ongoing patient support with real-time monitoring of complications and promotion of adherence through reminders, information and education.

Benefits:

Provision of the platform to network university hospitals and doctors in private practice, efficient specialist consultations enable rapid access to specific treatment and monitoring, closer networking enables faster start of treatment and a larger number of patients

Overview:

Digital identification of suitable participants and ongoing possible symptom queries using dedicated treatment pathways.

Benefits:

Simple and automated collection of relevant data, thanks to intelligent rules, study participants can be identified in a targeted manner, the digital companion enables continuous recording, even outside clinical settings, and thus the collection of real-world data

One solution. Everything you need.

Our full-service offering for medical device manufacturers combines dedicated digital treatment paths with extensive features for management and interaction with patients.

Patient Recruitment

Digital Companion

Interdisciplinary Care Networks

Real-world data for studies

Book an Appointment

Digital Care Made Easy. With myon.clinic.

No integration effort - get started right away!
Content can be adapted flexibly and in real time
Collection of structured real-world data
Interfaces to Withings, Apple Health and Google Fit
Automated monitoring - only possible with MDR IIa
Early detection of risks & side effects
Sustainable promotion of adherence
Improved patient satisfaction

 Make Health Scalable!​

Our Claim!

Quality & data security 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 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.​
Most of the standards and certifications mentioned here refer to the QMS and ISMS of ONCARE GmbH, which is responsible for the development of the myoncare healthcare platform. myon.clinic is a wholly owned subsidiary of ONCARE and builds its services on the myoncare healthcare platform. ​
FAQ​

We answer your questions about myon.clinic.

What is myon.clinic?

In which areas can myon.clinic be used?

What is a digital care pathway?

What is a class IIa medical device?

What are the technical requirements?