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DTSTART:19700308T020000
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BEGIN:VEVENT
DTSTAMP:20251016T135232Z
LOCATION:Grand C/D North
DTSTART;TZID=America/Chicago:20251014T113000
DTEND;TZID=America/Chicago:20251014T123000
UID:HFESAM_ASPIRE 2025_sess185@linklings.com
SUMMARY:HC2: Healthcare Human Factors Case Studies
DESCRIPTION:We are Here for your Seizure! Lessons Learned from Embedded Hu
 man Factors and Hospital Simulation to Design Processes for a New Epilepsy
  Monitoring Unit\n\nOur healthcare system aimed to enhance the usability a
 nd accuracy of seizure assessments in a new Epilepsy Monitoring Unit (EMU)
  by adapting a European seizure assessment tool. Using human factors engin
 eering (HFE) and translational simulation, we iteratively tested and refin
 ed the tool and work sys...\n\n\nMelinda Jamil, Kari Congenie, Bonnie Sati
 nover, and Abigail Magdaleno (Advocate Health)\n---------------------\nCan
  You Hear Me Now? Exploring In-Home Sound Levels and Device Design Inputs,
  from Data to Design\n\nRecent data collected from an in-home contextual-i
 nquiry actual-use study provided insight into sound levels in representati
 ve home settings during use of injection devices. These data are interpret
 ed alongside other published sources that characterize sound levels in hom
 e settings to tell a compreh...\n\n\nPati Anderson (Eli Lilly); Samantha C
 ombs (Eli Lilly and Company); Mikaylah Stumbo, Javad Eshraghi, Logan Armbr
 uster, and Anu Kadampelil (Eli Lilly); and Courtney Roberts (Bold Insight)
 \n---------------------\nAddressing Risk for Standalone Drug Products at t
 he Source\n\nIn recent years, many pharmaceutical companies have formed ro
 bust human factors teams to address changing regulatory requirements for a
 pplication of human factors engineering to medical devices and combination
  products. Since devices are the primary regulatory focus, stand-alone dru
 g products often ...\n\n\nNatalie Abts (Genentech)\n\nTrack: Health Care\n
 \nSession Chair: Alexandra Watral (Mayo Clinic)
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