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18 Nov 2019

18 Nov 2019


A straightforward method for meeting FDA Requirements for Design Inputs and Outputs     (15 Views)     

Event Serial No.-  WLD140701
Contact Person - Event Manager
Event inquiry /Organizer email address - traininngdotcom@gmail.com
Deadline for abstracts/proposals: 2019-11-16
Organized by: Traininng.com LLC View more Conference
Venue: Fremont,  CA,  United States of America

About Event

Overview A robust DIOM can serve as the foundation for meeting FDA requirements and is a useful tool to ensure future iterations, changes, and re-visits to the initial design are clearly documented. A DIOM ensures design information is clearly presented, well-documented, and most importantly, located within one simple document. This webinar provides a simplistic tool to help identify and categorize design inputs, determine the most effective method in providing design output evidence, and showing traceability to all activities associated with both.
Topic Covered: Engineering Teaching and Learning , Information Technology , Health , Public Health ,
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