The DIOM A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs 2019 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 2019 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
