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Laurence Sampson (Sr. Director Medical Device Business Processes, Siemens Digital Industries Software)
Date: Thursday, February 13
Time: 11:45 am - 1:00 pm
Track: Lunch & Learn
Vault Recording: TBD
Audience Level: All
How Risk Analysis can be combined with FMEA activities to provide complete traceability from user harms to production controls. When successfully constructed this method will provide you with a key to post-market surveillance and a solid foundation for progression to product design authoring applications.