CASE STUDY: Implementation of Risk Management for the Whole Life Cycle of Medical Devices

A session at 2nd Annual Software Design for Medical Devices Europe

  • Defining roles, responsibilities and activities in the whole Product Risk Management Process
  • Carefully documenting Risk Management Activities
  • Collecting and validating hazards: techniques and best practices
  • Effective handling of production and post-production information

Sign in to add slides, notes or videos to this session

Tell your friends!

View the schedule


See something wrong?

Report an issue with this session