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Human Factors for Medical Devices

October 6, 2015 - October 8, 2015

Highlights:

•  New guidance on preliminary analysis and formative testing
•  Learn the critical data approving authorities seek when assessing submissions
•  Participate in valuable walk-through ‘real world’ and ‘simulated’ exercises
•  Gain insights into meeting and surpassing HE-74, HE-75 and IEC-62366 standards
•  Open Q&A sessions with FDA representatives for medical and combination devices

Website: medical-device-regulations.com

Details

Start:
October 6, 2015
End:
October 8, 2015

Venue

Castleknock Hotel
Dublin, Ireland
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