Manufacturers

Create digital product companions in no time.

Our digital health platform empowers you to create personalized digital companion solutions that can support medication efficacy and improve data accessibility.

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myoncare for manufacturers

Digitally enhance analog products.

Create digital therapy and product companions to support doctors and patients from screening and diagnosis through to long-term therapy support.

Real-time symptom-monitoring

seamless patient support with real-time monitoring of symptoms and promotion of adherence through reminders and educational content.

Create intersectoral care networks

Connect relevant service providers involved in the care of patients treated with your products, enabling structured support throughout the entire patient journey.

Anonymized real-world data for studies & post-market surveillance

myoncare powers large‑scale, anonymized real‑world data collection to drive studies and meet post‑market surveillance needs.

Use cases for pharma and MedTech

Transform care and evidence generation with one intelligent platform

Empower physicians and patients to provide structured support throughout the entire patient journey, obtain anonymized real-world data for studies and post-market surveillance, and automate your study processes—all in one data-driven ecosystem.

Disease management

Streamline patient care within interdisciplinary networks and manage diseases smarter through data-driven interventions

Therapy companion

Guide patients step-by-step through complex treatments with symptom tracking, personalized content and reminders.

Real-world evidence

Transform routine care data into actionable insights to drive research, reimbursement, and quality-based outcomes.

Clinical trial companion

Digitally manage study participants, ePROs, and visit schedules to ensure compliance and data integrity across sites.

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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​

We answer your questions
about myoncare

What is myoncare ?

How can myoncare help me? ​

In which areas can myoncare be used?  ​

How does the content management system work?  ​

The content management system is the heart of myoncare. Using the CMS, content can be easily created, stored with automation rules and combined into treatment paths. The user interface of the CMS has been designed to be particularly intuitive so that it can also be easily operated by users without programming knowledge.

I don't have time to create content myself, is there a solution for this? ​

What does Class IIa medical device mean? What are the advantages?  ​

What are the technical requirements?​