Innovation and Technology Saving Lives

The medical technology sector in Germany is strongly characterized by growth, innovation and intensive use of technology. It provides a substantial contribution to efficient health care. However, enterprises are facing ever more government regulations, increa- sing complexity and growing costs in long-term development processes.

Utilization of technology is welcomed in medical technology as in hardly any other sector. Since these products do not only improve the quality of living but even save and sustain lives in many cases. However, the development of such medical technology products causes difficulties for enterprises owing to the very short product life cycles of less than 3 years required in many cases. The overall development process – from the very first idea to the final medical product – tends to become longer, more complex and often more cost-intensive.

Scope of Services

  • System and software development in accordance with IEC 62304

  • Development of operating concepts for medical technology devices

  • Software development for minimally invasive surgery

  • Prototype development

  • Requirements engineering

  • Integration and system testing



Safety and Performance Are Key Aspects

Medical products require comprehensive technical and clinical testing before they are approved for further trials and finally application on patients. The protection and well-being of the patient have top priority. This means for the use of technical products or systems that they are subject to maximum safety requirements and testing as well as a strict quality management system.

Competent Support at any Stage

This is where we come into play. Our long-term experience in the development of complex systems enables us to support you in any phase of development. We support your complete development process as a competent partner.

Medizintechnik - System

Experience and Competencies

Systems engineering
  • Requirements management at system level

  • System architecture and design

  • Analysis and consulting for the selection of software components for runtime environments

Software development
  • Software requirements management
  • Software architecture
  • Software module design and implementation
Verification and validation
  • Preparation of module and unit testing

  • Software integration and system testing

  • Preparation of the test documentation for module, integration and system tests

  • Creating automated test sequences at module and sub-integration levels

  • Validation

    • System requirements

    • Software requirements

Support processes
  • Project management

  • Quality assurance

  • Configuration management for subcomponents

  • Problem and change management

  • Documentation

  • V-Model

  • IEC 62304

  • EN ISO 13485

Tool experience (synopsis)
  • Enterprise Architect

  • Qt creator, Qt quick und Qt widget

  • Qt QML; C, C++

  • MariaDB

  • C#, WPF, .NET

  • git

  • Doxygen

  • Jira, confluence, Seapine Test track

  • alfresco

  • vera++, cppcheck

  • Yocto – ubuntu

  • Diverse Microcontroller

Examples from the project world
  • Touch interface product development for users involving user profiles in the lab environment

  • Supportforusecaseandstakeholderanalyses for product optimization geared to market requirements

  • Interfacing/communication with other components of the overall system

  • Support for resource optimization in runtime environments

  • Preparation and realization of component and system tests

  • Product development for minimally invasive surgery using a robot arm

  • Low-level software development at microcontroller level

  • Implementation and integration of boot loaders

  • Runtime optimization

  • Working out safety maintenance concepts

  • Implementationofvariousinterfaceprotocols

Marco Moosmann

Do you have any questions about medical technology?

Marco Moosmann
Key Account Manager

+49 7532 4466-251

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