This course will give an introduction how to develop medical software under the requirements of the ISO 62304 and how to apply these in a medical software development project and how a smart application during the medical software development and in the post market process is possible. Further the risk management of medical software development. In the European Union is the application of the ISO 62304 for medical software mandatory and part of the essential requirements of the medical device regulation. In the technical documentation is required to approve the development process and the life cycle of medical software according ISO 62304. (from )

complianceonline.com/learn-iso-62304-standard-implementation-in-medical-software-development-project-zurich-seminar-training-80607SEM-prdsm?channel=eleventary

• This event has passed.
  Through March 5, 2019

  March 4, 2019 to March 5, 2019
• Zurich, Switzerland
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• Contact Ashutos Swain for more information
  8887172436 or [email protected]
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