No-code CMS. Class IIa medical device.

Build your solution
on myoncare!

And avoids high costs and the expense of in-house development and certification. Let's Build Launch your Medical App
Benefits

myoncare is your strong partner!

No matter whether you need an advanced infrastructure for an existing solution or want to realize a new idea quickly and cost-effectively.1
Test your Medical App
  • tick Icon Class IIa medical device
  • ISO Icon ISO 27001 certified QMS of ONCARE
  • no code CMS No-Code Content Management System
  • Rich Content Icon Numerous features for content creation
  • Development Icon Continuous further development since 2015
  • Server Icon Hosted on servers in Germany
  • Excellence Icon Already numerous successful projects
  • Integration Icon Interfaces to Withings, Apple Health and Google Fit
No-code CMS

Create your own care pathways
in just a few steps!

CREATE!

Individual content (e.g. health questions) can be entered individually and easily combined into components (e.g. health questionnaire) using drag-and-drop.

Create Example
Example Chart

COMBINE!

Automate your content by predefining the playout of components based on time intervals or responses given.

BE SMART!

Store your care pathways with direct alarm rules or scores that are automatically calculated based on the answers given.

Example Chart 2
Rocket Launch

READY TO GO!

After finalizing your treatment pathway, you can simply share it with users via QR code or integrate it on your own website.2

Community

Become part of our Medical Content Creator Community!

Derma2go Logo
Hartmann Logo
Roche Logo
Universitats klinikumbonn Logo
Uniklinikum Wurzburg Logo
Strahlentherapie Sud Logo
Augsgurg Logo
Recare Logo
Frieburg Logo
Diakovere Logo
MDR IIA Certification

Save yourself the time-consuming certification process.

Medical device software that previously belonged to Class I will, with a few exceptions, fall into at least Class IIa in future. This primarily affects software that is intended to provide information that is used to make decisions for diagnostic or therapeutic purposes.

That's the cost of MDR IIa certification:

  • Manufacturers must establish a quality management system certified in accordance with DIN EN ISO 13485.
  • Strict requirements apply to clinical trials, market surveillance and incident reporting.
  • Detailed technical documentation is essential, including comprehensive safety and performance certificates.
Next steps

myoncare helps you to get started with your project!

Our team will discuss your project idea with you. Book your non-binding consultation appointment now!

1With myoncare you can create digital treatment pathways. ONCARE GmbH does not provide any certification services for you. With myoncare, you can only use digital treatment pathways within the scope of the intended purpose of myoncare. For example, myoncare may not be used for emergencies. For patient monitoring and diagnostic support, myoncare may currently only be used by healthcare professionals. Please contact sales@myoncare.com to find out more about myoncare and the possibilities for your project solution.

2Not all care pathways created are suitable for publication.

myoncare is a CE-marked Class Iia medical device. 0123

Rx only. Medical Device Data System. The FDA has recommended enforcement discretion for this device.