Target Group

The CPMS initiative primarily addresses those entrusted with the development and quality assurance of software as an accessory of medical devices and as a stand-alone medical device. With certain limitations, this also applies to software for the pharmaceutical/GxP sector.


Among others the initiative particularly appeals to

  • Software developers working for manufacturers of medical devices and clinical information systems and their service providers
  • Product manager
  • Project managers
  • Regulatory affairs managers
  • Quality managers
  • Auditors and employees of notified bodies
  • Employees of monitoring agencies such as regional authorities and trade supervisory boards