ELECTRONICS / SOFTWARE

DMT Produktentwicklung GmbH (Nufringen - DE)

  • Experience with regulatory standards (ISO 13485, ISO 14971, IEC 60601-1, IEC 62304, IEC 62366-1)
  • Experience in the hardware and software development of medical-/in-vitro-diagnostic-products
  • Design and construction of system architectures
  • Definition of assembly specification
  • Medical device software according to IEC 62304
  • Development of electronic assemblies and components
  • Documentation according to medical technology standards
  • Software tests such as code reviews, static code analysis, unit tests or verification of complete software systems and electronic assemblies

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