The DIOM – A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs 2019
20 Mar 2019
Webinar
Description
Topics
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
Who should Attend
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
Past Events
The DIOM – A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs 2019 - 20 Mar 2019, Webinar (82847)
Important
Please, check "The DIOM – A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs" official website for possible changes, before making any traveling arrangements
