Apologies for the delayed response. There should be a zoom link sent with registration. The educational portion of the event will be available through that zoom link. If this is not the case I will work RAPS headquarters to get you a zoom link.
Original Message:
Sent: 02-Feb-2024 17:01
From: Sara Coon
Subject: [Upcoming Hybrid Chapter Event] Human Factors Evaluations and Medical Devices
The title states Hybrid Chapter Event. The registration looks like it is in-person only. Please clarify what is meant by Hybrid.
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Sara Coon
Director, Regulatory Affairs
Halozyme Therapeutics Inc.
MN United States
Original Message:
Sent: 29-Jan-2024 20:10
From: Danielle Pennant
Subject: [Upcoming Hybrid Chapter Event] Human Factors Evaluations and Medical Devices
Tuesday, 20 Feb 2024 (11:00 AM - 01:30 PM) Central Time (US & Canada)
1.0 RAC Credit
The Twin Cities Chapter is hosting a Hybrid Event - hope you can join us!
Applying human factors principles during early medical device development is often minimized, overlooked, or delayed until product validation. These approaches may miss opportunities to comprehensively understand the device's usability risks and resolve them to ensure its safe use before it enters the marketplace. Learn from a human factor expert about the systematic lifecycle processes to apply human factors principles and usability engineering that meet and will go beyond the FDA requirements for human factors.
Click here to register today!
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Danielle Pennant
Chapter Event Specialist
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