The DIOM – A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs

The DIOM – A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs is a webinar that covers topics such as:

  • Better understanding of FDA regulations with regards to design input and output
  • Introduction to the DIOM template
  • An organized approach in meeting design input and output requirements
  • How to identify your design inputs
  • Ways in which design inputs can be verified
  • How to categorize your design inputs and their sources
  • Common documents and activities used as design output evidence
  • A simplified way to ensure design inputs and outputs are continually maintained and tracked
  • Additional requirements of design inputs and outputs

The DIOM – A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs is intended for:

  • Quality Control Departments
  • Quality Assurance Departments
  • Regulatory Affairs Departments
  • Research and Development Departments
  • Engineering Departments
  • Manufacturing Departments
  • Production Departments
  • Operations Departments
  • Internal Auditors
  • Software Developers and Managers
  • IT Managers and System Administrators
  • Design Engineers
  • Software Test Personnel
  • Software Quality Personnel
  • Software Validation Engineers

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